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3528079 | VfR Bürstadt | https://en.wikipedia.org/w/index.php?title=VfR%20Bürstadt | VfR Bürstadt
is one of the relatively few German clubs that have sold their naming rights to an outside sponsor, an arrangement that ended with the bankruptcy of OLI in 1982.
Their run of success ended in the 1990s with a series of poor finishes in the Amateur Oberliga Hessen (III) early in the decade. Beginning with the 1993–94 season, they bounced between the Oberliga Hessen (IV) and Landesliga Hessen-Süd (V) for nearly a decade before finally collapsing in 2002 and voluntarily accepting relegation all the way down to Bezirksliga (VII).
After a drop to the ninth tier in 2008–09 the club has recovered again and moved back up to the Gruppenliga (VII) in 2011–12, followed by promotion to the Verbandsliga | 6,125,400 |
3528079 | VfR Bürstadt | https://en.wikipedia.org/w/index.php?title=VfR%20Bürstadt | VfR Bürstadt
in 2013. The team won the league title in the Verbandsliga in 2014 as well but, instead of accepting promotion to the Hessenliga the club withdrew to the tier eight Kreisoberliga Bergstraße instead for financial reasons.
# Honours.
The club's honours:
## League.
- German amateur championship
- Champions: 1975
- Oberliga Hessen
- Champions: 1972, 1977, 1979, 1983, 1984
- Runners-up: 1982, 1986
- Landesliga Hessen-Süd
- Champions: 2001
- Runners-up: 1997
- Verbandsliga Hessen-Süd
- Champions: 2014
- Gruppenliga Darmstadt
- Champions: 2013
## Cup.
- Hesse Cup
- Winners: 1975, 1977
# Recent seasons.
The recent season-by-season performance of the club:
- With the introduction | 6,125,401 |
3528079 | VfR Bürstadt | https://en.wikipedia.org/w/index.php?title=VfR%20Bürstadt | VfR Bürstadt
hampions: 2013
## Cup.
- Hesse Cup
- Winners: 1975, 1977
# Recent seasons.
The recent season-by-season performance of the club:
- With the introduction of the Regionalligas in 1994 and the 3. Liga in 2008 as the new third tier, below the 2. Bundesliga, all leagues below dropped one tier. Also in 2008, a large number of football leagues in Hesse were renamed, with the Oberliga Hessen becoming the Hessenliga, the Landesliga becoming the Verbandsliga, the Bezirksoberliga becoming the Gruppenliga and the Bezirksliga becoming the Kreisoberliga.
# External links.
- Official website
- The Abseits Guide to German Soccer
- Das deutsche Fußball-Archiv historical German domestic league tables | 6,125,402 |
3528082 | Fredless | https://en.wikipedia.org/w/index.php?title=Fredless | Fredless
Fredless
"Fredless" is episode 5 of season 3 in the television show "Angel". Written by Mere Smith and directed by Marita Grabiak, it was originally broadcast on October 22, 2001 on the WB network. Fred's parents, Roger and Trish Burkle, arrive in town from Texas to take her home with them, prompting Fred to run away. Angel learns that Fred's problems with her mother and father are purely emotional while Mr. and Mrs. Burkle prove themselves to be formidable fighters against demons. Meanwhile, the gang is unknowingly in danger after Angel beheads a vicious demon whose head is the breeding ground for a strain of insect demons, causing a swarm of giant cockroaches to lay siege to the hotel in order | 6,125,403 |
3528082 | Fredless | https://en.wikipedia.org/w/index.php?title=Fredless | Fredless
to retrieve their offspring.
# Plot.
Fred asks about Angel's relationship with Buffy, curious because he left so abruptly to meet her at the end of the previous episode. Cordelia and Wesley put on an overly-dramatic, humorous play that summarizes what Angel and Buffy's off-screen reunion might have been like. When Angel returns, he invites Fred out to ice cream, but ends up tracking a Durslar demon into the sewers. Fred notices some crystal formations on the sewer wall before Angel sends her back to the Hyperion Hotel for safety.
The gang reorganize the weapons cabinet, bored and anxious for a job. Cordelia discovers an object that could be a weapon or a toaster that Fred was making. A couple, | 6,125,404 |
3528082 | Fredless | https://en.wikipedia.org/w/index.php?title=Fredless | Fredless
Roger and Trish Burkle, enter the hotel searching for assistance in finding their lost daughter, Fred, whom another private detective traced to Angel Investigations. The Burkles are oblivious to the supernatural so Cordelia, Wesley, and Gunn lie about Fred's disappearance and their work. When Fred returns and sees the couple in the lobby, she dashes upstairs unseen. She tries to erase the writing she scribbled over her bedroom walls, then leaves the hotel.
Angel returns with the severed head of the Durslar demon and is introduced to the Burkles as their associate who also works in movies, hence the "fake" demon head. They all head upstairs, but find her room empty. While the Burkles wait out | 6,125,405 |
3528082 | Fredless | https://en.wikipedia.org/w/index.php?title=Fredless | Fredless
in the lobby, Angel and crew converse about the possible reasons for Fred to run away from her parents and whether the Burkles are being completely honest. They join the Burkles again and everyone splits up to find her.
After roaming the streets alone, Fred ends up at Caritas and tries to get help from Lorne, who is bitter about the recent fight that destroyed much of his bar. She sings without provocation and exposes her obvious fear and panic to him. He knows what she's running from and she doesn't realize she's strong enough to face it.
Eventually, the rest of the gang end up at Caritas, but Lorne refuses to play along with attempts to keep the Burkles oblivious to demonic activity and | 6,125,406 |
3528082 | Fredless | https://en.wikipedia.org/w/index.php?title=Fredless | Fredless
expresses his distaste for being used all the time. Finally, Lorne reveals that Fred is at the bus station. When her family and friends show up, Fred doesn't want to admit that her parents are real because it means her awful experience in Pylea was real, but finally breaks down. Just then, a giant bug demon that followed Angel from the sewers attacks the group. Weaponless, Angel tries to handle the demon alone; all attempts to hide the truth from the Burkles are forgotten as the group rushes to Gunn's truck for fighting tools. Angel continues the fight with the bug demon until Trish Burkle kills it by driving a bus into it.
Back at the hotel, Fred notices the crystals she saw in the sewers | 6,125,407 |
3528082 | Fredless | https://en.wikipedia.org/w/index.php?title=Fredless | Fredless
on the Durslar's head. Fred wonders about her place in the gang while her parents are just grateful to have their daughter back. They reveal how they were prepared to call the police, thinking Angel and friends kidnapped their daughter. She decides that she wants to go home with her parents because she doesn't really belong with the rest of the group. As Fred packs, she tells Angel she wrote her life story on her bedroom wall.
After Fred leaves with her parents, many bug demons begin to show up at the hotel. Fred, who has realized in the cab that the cockroach demons would return, rushes back to deploy her toaster weapon, sending an ax flying at the severed demon head. The head splits open, | 6,125,408 |
3528082 | Fredless | https://en.wikipedia.org/w/index.php?title=Fredless | Fredless
releasing little bugs that the other demons collect before departing. Fred explains how she realized the little crystals were dried ichor from the bug demon, indicating a connection between it and the severed head. Fred decides she does have a place at Angel Investigations after all, and invites everyone up to her room, where they help her paint the walls. Fred paints over a picture she drew of her and Angel on the horse from Pylea.
# Production.
Fred's mother mentions her husband fell asleep while watching the film "", which was written by series creator Joss Whedon.
## Arc significance.
- This episode marks Fred's cementation into the main group. Up until this point, it was uncertain if | 6,125,409 |
3528082 | Fredless | https://en.wikipedia.org/w/index.php?title=Fredless | Fredless
Fred's run on the show would mimic Doyle's, in which Joss Whedon had Glenn Quinn in the title credits only for 10 episodes until he let Doyle's character go.
- Angel and Buffy's meeting, which is never shown on screen, is the subject of a comic by "Buffy" writer Jane Espenson called "Reunion".
# Cultural References.
- Near the end of the episode Fred's mother is talking to Cordelia About how Fred's father loves the Alien movies, then she says "Except for the last one, I think he dozed off" She's referring to Alien Resurrection which was written by Joss Whedon.
# Reception.
UGO Networks called this episode the season's low point, because it "mines the 'dreaded parental visit' plotline." | 6,125,410 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
ICD-10 is an international statistical classification used in health care and related industries.
Produced by the World Health Organization, it is used in several countries around the world. Some have gone on to develop their own national enhancements, building off the international version of the classification.
Chapter XVI of ICD-10 deals with conditions effecting the perinatal period. Examples of conditions captured using codes from Chapter XVI include; birth injuries, prematurity, neonatal jaundice, and neonatal withdrawal.
For coding and reporting purposes the perinatal period is defined as before birth through | 6,125,411 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
the 28th day following birth.
# P00–P96 – Certain conditions originating in the perinatal period.
## (P00–P04) Fetus and newborn affected by maternal factors and by complications of pregnancy, labour and delivery.
- () Fetus and newborn affected by maternal conditions that may be unrelated to present pregnancy
- () Fetus and newborn affected by maternal complications of pregnancy
- () Fetus and newborn affected by complications of placenta, cord and membranes
- () Fetus and newborn affected by placenta praevia
- () Fetus and newborn affected by other forms of placental separation and haemorrhage
- () Fetus and newborn affected by other and unspecified morphological and functional abnormalities | 6,125,412 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
of placenta
- () Fetus and newborn affected by placental transfusion syndromes
- Placental and cord abnormalities resulting in twin-to-twin or other transplacental transfusion
- () Fetus and newborn affected by prolapsed cord
- () Fetus and newborn affected by other compression of umbilical cord
- () Fetus and newborn affected by other and unspecified conditions of umbilical cord
- () Fetus and newborn affected by chorioamnionitis
- () Fetus and newborn affected by other abnormalities of membranes
- () Fetus and newborn affected by abnormality of membranes, unspecified
- () Fetus and newborn affected by other complications of labour and delivery
- () Fetus and newborn affected by noxious | 6,125,413 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
influences transmitted via placenta or breast milk
## (P05–P08) Disorders related to length of gestation and fetal growth.
- () Slow fetal growth and fetal malnutrition
- () Light for gestational age
- () Small for gestational age
- () Fetal malnutrition without mention of light or small for gestational age
- () Slow fetal growth, unspecified
- Fetal growth retardation NOS
- () Disorders related to short gestation and low birth weight, not elsewhere classified
- () Extremely low birth weight
- () Other low birth weight
- () Extreme immaturity
- () Other preterm infants
- Prematurity NOS
- () Disorders related to long gestation and high birth weight
- () Exceptionally large baby
- | 6,125,414 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
() Other heavy for gestational age infants
- () Post-term infant, not heavy for gestational age
- Postmaturity NOS
## (P10–P15) Birth trauma.
- () Intracranial laceration and haemorrhage due to birth injury
- () Subdural haemorrhage due to birth injury
- () Cerebral haemorrhage due to birth injury
- () Intraventricular haemorrhage due to birth injury
- () Subarachnoid haemorrhage due to birth injury
- () Tentorial tear due to birth injury
- () Other intracranial lacerations and haemorrhages due to birth injury
- () Unspecified intracranial laceration and haemorrhage due to birth injury
- () Other birth injuries to central nervous system
- () Birth injury to scalp
- () Cephalhaematoma | 6,125,415 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
due to birth injury
- () Chignon due to birth injury
- () Epicranial subaponeurotic haemorrhage due to birth injury
- () Bruising of scalp due to birth injury
- () Monitoring injury of scalp of newborn
- () Other birth injuries to scalp
- () Birth injury to scalp, unspecified
- () Birth injury to skeleton
- () Birth injury to peripheral nervous system
- () Erb's paralysis due to birth injury
- () Klumpke's paralysis due to birth injury
- () Phrenic nerve paralysis due to birth injury
- () Other brachial plexus birth injuries
- () Birth injuries to other parts of peripheral nervous system
- () Birth injury to peripheral nervous system, unspecified
- () Other birth injuries
## | 6,125,416 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
(P20–P29) Respiratory and cardiovascular disorders specific to the perinatal period.
- () Intrauterine hypoxia
- () Birth asphyxia
- () Respiratory distress of newborn
- () Respiratory distress syndrome
- () Transient tachypnoea of newborn
- () Congenital pneumonia
- () Congenital pneumonia due to viral agent
- () Congenital pneumonia due to Chlamydia
- () Congenital pneumonia due to staphylococcus
- () Congenital pneumonia due to streptococcus, group B
- () Congenital pneumonia due to Escherichia coli
- () Congenital pneumonia due to Pseudomonas
- () Congenital pneumonia due to other bacterial agents
- Haemophilus influenzae
- Klebsiella pneumoniae
- Mycoplasma
- Streptococcus, | 6,125,417 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
except group B
- () Congenital pneumonia due to other organisms
- () Congenital pneumonia, unspecified
- () Neonatal aspiration syndromes
- () Neonatal aspiration of meconium
- () Interstitial emphysema and related conditions originating in the perinatal period
- () Interstitial emphysema originating in the perinatal period
- () Pneumothorax originating in the perinatal period
- () Pneumomediastinum originating in the perinatal period
- () Pneumopericardium originating in the perinatal period
- () Other conditions related to interstitial emphysema originating in the perinatal period
- () Pulmonary haemorrhage originating in the perinatal period
- () Chronic respiratory disease originating | 6,125,418 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
in the perinatal period
- () Wilson-Mikity syndrome
- () Bronchopulmonary dysplasia originating in the perinatal period
- () Other chronic respiratory diseases originating in the perinatal period
- () Unspecified chronic respiratory disease originating in the perinatal period
- () Other respiratory conditions originating in the perinatal period
- () Cardiovascular disorders originating in the perinatal period
- () Neonatal cardiac failure
- () Neonatal cardiac dysrhythmia
- () Neonatal hypertension
- () Persistent fetal circulation
- () Transient myocardial ischaemia of newborn
- () Other cardiovascular disorders originating in the perinatal period
- () Cardiovascular disorder originating | 6,125,419 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
in the perinatal period, unspecified
## (P35–P39) Infections specific to the perinatal period.
- () Congenital viral diseases
- () Congenital rubella syndrome
- () Congenital cytomegalovirus infection
- () Congenital herpesviral infection (herpes simplex)
- () Congenital viral hepatitis
- () Other congenital viral diseases
- () Congenital viral disease, unspecified
- () Bacterial sepsis of newborn
- () Sepsis of newborn due to streptococcus, group B
- () Sepsis of newborn due to other and unspecified streptococci
- () Sepsis of newborn due to Staphylococcus aureus
- () Sepsis of newborn due to other and unspecified staphylococci
- () Sepsis of newborn due to Escherichia coli
- | 6,125,420 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
() Sepsis of newborn due to anaerobes
- () Other bacterial sepsis of newborn
- () Bacterial sepsis of newborn, unspecified
- () Other congenital infectious and parasitic diseases
- () Congenital tuberculosis
- () Congenital toxoplasmosis
- () Neonatal listeriosis (disseminated)
- () Congenital falciparum malaria
- () Other congenital malaria
- () Neonatal candidiasis
- () Other specified congenital infectious and parasitic diseases
- () Congenital infectious and parasitic disease, unspecified
- () Omphalitis of newborn with or without mild haemorrhage
- () Other infections specific to the perinatal period
- () Neonatal infective mastitis
- () Neonatal conjunctivitis and dacryocystitis
- | 6,125,421 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
() Intra-amniotic infection of fetus, not elsewhere classified
- () Neonatal urinary tract infection
- () Neonatal skin infection
- () Other specified infections specific to the perinatal period
- () Infection specific to the perinatal period, unspecified
## (P50–P61) Haemorrhagic and haematological disorders of fetus and newborn.
- () Fetal blood loss
- () Fetal blood loss from vasa praevia
- () Fetal blood loss from ruptured cord
- () Fetal blood loss from placenta
- () Twin-to-twin transfusion syndrome
- () Fetal-maternal haemorrhage
- () Fetal blood loss from cut end of co-twin's cord
- () Other fetal blood loss
- () Fetal blood loss, unspecified
- () Umbilical haemorrhage | 6,125,422 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
of newborn
- () Intracranial nontraumatic haemorrhage of fetus and newborn
- () Haemorrhagic disease of fetus and newborn
- () Other neonatal haemorrhages
- () Haemolytic disease of fetus and newborn
- () Rh isoimmunization of fetus and newborn
- () ABO isoimmunization of fetus and newborn
- () Other haemolytic diseases of fetus and newborn
- () Haemolytic disease of fetus and newborn, unspecified
- () Hydrops fetalis due to haemolytic disease
- () Kernicterus
- () Neonatal jaundice due to other excessive haemolysis
- () Neonatal jaundice from other and unspecified causes
- () Disseminated intravascular coagulation of fetus and newborn
- () Other perinatal haematological disorders
- | 6,125,423 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
() Neonatal alloimmune thrombocytopenia
- () Polycythaemia neonatorum
- () Anaemia of prematurity
- () Congenital anaemia from fetal blood loss
- () Other congenital anaemias, not elsewhere classified
- () Transient neonatal neutropenia
- () Other transient neonatal disorders of coagulation
- () Other specified perinatal haematological disorders
- () Perinatal haematological disorder, unspecified
## (P70–P74) Transitory endocrine and metabolic disorders specific to fetus and newborn.
- () Transitory disorders of carbohydrate metabolism specific to fetus and newborn
- () Transitory neonatal disorders of calcium and magnesium metabolism
- () Other transitory neonatal endocrine disorders
- | 6,125,424 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
() Other transitory neonatal electrolyte and metabolic disturbances
## (P75–P78) Digestive system disorders of fetus and newborn.
- () Meconium ileus
- () Other intestinal obstruction of newborn
- () Necrotizing enterocolitis of fetus and newborn
- () Other perinatal digestive system disorders
- () Perinatal intestinal perforation
- Meconium peritonitis
- () Other neonatal peritonitis
- () Neonatal haematemesis and melaena due to swallowed maternal blood
- () Noninfective neonatal diarrhoea
- () Other specified perinatal digestive system disorders
- () Perinatal digestive system disorder
## (P80–P83) Conditions involving the integument and temperature regulation of fetus and newborn.
- | 6,125,425 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
() Hypothermia of newborn
- () Other disturbances of temperature regulation of newborn
- () Other conditions of integument specific to fetus and newborn
- () Sclerema neonatorum
- () Neonatal erythema toxicum
- () Hydrops fetalis not due to haemolytic disease
- () Other and unspecified oedema specific to fetus and newborn
- () Breast engorgement of newborn
- () Congenital hydrocele
- () Umbilical polyp of newborn
- () Other specified conditions of integument specific to fetus and newborn
- () Condition of integument specific to fetus and newborn, unspecified
## (P90–P96) Other disorders originating in the perinatal period.
- () Convulsions of newborn
- () Other disturbances of | 6,125,426 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
cerebral status of newborn
- () Neonatal cerebral ischaemia
- () Acquired periventricular cysts of newborn
- () Neonatal cerebral leukomalacia
- () Neonatal cerebral irritability
- () Neonatal cerebral depression
- () Neonatal coma
- () Hypoxic ischaemic encephalopathy of newborn
- () Other specified disturbances of cerebral status of newborn
- () Disturbance of cerebral status of newborn, unspecified
- () Feeding problems of newborn
- () Reactions and intoxications due to drugs administered to fetus and newborn
- () Disorders of muscle tone of newborn
- () Transient neonatal myasthenia gravis
- () Congenital hypertonia
- () Congenital hypotonia
- Nonspecific floppy baby syndrome
- | 6,125,427 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
() Other disorders of muscle tone of newborn
- () Disorder of muscle tone of newborn, unspecified
- () Fetal death of unspecified cause
- Deadborn fetus NOS
- Stillbirth NOS
- () Other conditions originating in the perinatal period
- () Congenital renal failure
- () Neonatal withdrawal symptoms from maternal use of drugs of addiction
- () Withdrawal symptoms from therapeutic use of drugs in newborn
- () Wide cranial sutures of newborn
- () Termination of pregnancy, fetus and newborn
- () Complications of intrauterine procedures, not elsewhere classified
- () Other specified conditions originating in the perinatal period
- () Condition originating in the perinatal period, unspecified
- | 6,125,428 |
3528096 | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVI:%20Certain%20conditions%20originating%20in%20the%20perinatal%20period | ICD-10 Chapter XVI: Certain conditions originating in the perinatal period
newborn
- () Termination of pregnancy, fetus and newborn
- () Complications of intrauterine procedures, not elsewhere classified
- () Other specified conditions originating in the perinatal period
- () Condition originating in the perinatal period, unspecified
- Congenital debility NOS
# Excludes.
- Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- Endocrine, nutritional, and metabolic diseases (E00-E88)
- Injury, poisoning and certain other consequences of external causes (S00-T88)
- Neoplasms (C00-D49)
- Tetanus neonatorum (A33)
# See also.
- List of ICD-10 codes
- International Statistical Classification of Diseases and Related Health Problems | 6,125,429 |
3528095 | Billy (Angel) | https://en.wikipedia.org/w/index.php?title=Billy%20(Angel) | Billy (Angel)
Billy (Angel)
"Billy" is episode 6 of season 3 in the television show "Angel". Written by Tim Minear and Jeffrey Bell and directed by David Grossman, it was originally broadcast on October 29, 2001 on the WB television network. In this episode, Angel investigates a wave of violence against women throughout Los Angeles, caused by Billy's ability to infect men with murderous misogyny. Cordelia seeks the aid of Lilah, who is a victim of Billy’s power, while Fred finds herself in danger from an infected Wesley.The song Clint Eastwood by Gorillaz is played in the episode.
# Plot.
Angel teaches Cordelia how to sword fight so that she can defend herself if Angel isn't there to protect her. Due to | 6,125,430 |
3528095 | Billy (Angel) | https://en.wikipedia.org/w/index.php?title=Billy%20(Angel) | Billy (Angel)
her cheerleading experience, she is a fast study. Lilah finds Billy (the man Angel was forced to rescue from a fiery hell dimension by the lawyers of Wolfram & Hart in "That Vision Thing") in her office talking with Gavin Park. The influential Congressman Blim, Billy's uncle, arrives to take the young man home. After Billy and the congressman leave, Lilah tells Gavin to stay away from her clients. Gavin isn't interested in her suggestions and suddenly attacks her, smashing her head into a glass case and strangling her.
Cordy and Wesley discuss Cordelia's training with Angel, and Wesley suggests he train Fred, leading Cordelia to inquire about his romantic feelings for Fred. She suggests that | 6,125,431 |
3528095 | Billy (Angel) | https://en.wikipedia.org/w/index.php?title=Billy%20(Angel) | Billy (Angel)
he ask her out, but their conversation is cut short by a vision of a woman being beaten by her husband in a convenience store. Strangely, the event occurred a week ago and the woman is now dead. Wesley learns that the husband's explanation for killing his wife was simply that "she wouldn't stop talking" and gets surveillance photos from the crime, in which they spot Billy. After learning that Angel freed Billy to save her, Cordelia feels responsible for the woman's death, but Angel assures her the blame belongs to Lilah. He visits Lilah at her apartment and is shocked to find her badly beaten. She says Billy is untouchable due to his political connections. Wesley, Gunn, and Angel track down | 6,125,432 |
3528095 | Billy (Angel) | https://en.wikipedia.org/w/index.php?title=Billy%20(Angel) | Billy (Angel)
Billy; however, the police arrive first to take Billy into custody for phoning in a tip on the location of a murder victim. Before he's taken away, Billy touches one of the officers on the arm. Later in the squad car, Sanchez's female partner doesn't take the route he tells her to, causing him to get angry and hit her repeatedly. Fred relays information from a police scanner, saying that Billy got away before arriving at the station. It is later discovered that after being hit by her partner, the female cop shot him and is now resting in the hospital. At the scene of the crime, Angel realizes that some of the blood is Billy's, and Wesley takes a sample of his blood to examine at the hotel.
Cordelia | 6,125,433 |
3528095 | Billy (Angel) | https://en.wikipedia.org/w/index.php?title=Billy%20(Angel) | Billy (Angel)
goes to Lilah's to demand information, and Lilah explains that Billy's touch turns men into vicious misogynists, though the effect varies from male to male. Wesley returns to the hotel and Fred helps him examine Billy's blood cells through the microscope and observes that his power is in his blood, saliva, and sweat. Wesley begins to act hostile towards Fred, and when she runs from the office, he catches her and tosses her face-first into the stairs. He stalks her through the hotel with an axe in his hand. As she runs, she is caught by Gunn and taken into one of the bedrooms.
Following reports of misogynistic violence, Angel tracks Billy's last location to a party at his cousin's house, where | 6,125,434 |
3528095 | Billy (Angel) | https://en.wikipedia.org/w/index.php?title=Billy%20(Angel) | Billy (Angel)
he discovers that Billy's entire family is aware of his situation and want him gone. Cordelia finds Billy waiting for a private plane at the airport. He's not interested in talking with her, and she isn't either, debilitating him with a stun gun to his groin. Angel arrives to help Cordelia, and Billy touches Angel's face.
In the bedroom, Gunn realizes that he too has been infected after touching the bloody paper down in the lobby. He tries to leave, but Wesley is blocking the door, so Gunn has Fred knock him unconscious. Wesley breaks into the room, insulting Fred as he advances toward her. She pulls a rope which sends a fire extinguisher flying down to hit Wesley in the face and send him falling | 6,125,435 |
3528095 | Billy (Angel) | https://en.wikipedia.org/w/index.php?title=Billy%20(Angel) | Billy (Angel)
through a hole in the floor. Meanwhile, at the airport, Angel turns on Billy and hits him, explaining that Billy's power doesn't affect him. As Angel and Billy fight, Lilah shoots Billy dead before Cordelia can get a clear shot with her crossbow.
Days later, Cordelia and Angel continue with their training, as Angel reveals that the reason he wasn't affected by Billy's touch was that he left behind the capacity to hate long ago. Meanwhile, Wesley, who has kept to himself since the incident, receives a visit from Fred. She doesn't blame him for what happened, but he blames himself. Concerned that violence is a part of him, he doesn't know who he is or how to return to life as it was before. Fred | 6,125,436 |
3528095 | Billy (Angel) | https://en.wikipedia.org/w/index.php?title=Billy%20(Angel) | Billy (Angel)
says he's needed at the office and insists that she knows he had no control over what happened. Fred leaves when Wesley agrees to return to the office. As the door closes, she can hear him crying on the other side.
# Production.
The episode invokes the Kennedy Family---who also have prominent political connections. William Kennedy Smith was a nephew of former Senator Edward Kennedy and was accused of sexually assaulting a woman in a 1991 Palm Beach Florida case. Smith was acquitted of the charges.
Dylan Blim invokes John F. Kennedy Jr. who was a member of the family himself—but adamantly disliked the conduct of relatives. Dylan is aware that Angel is a vampire with a good potential to kill | 6,125,437 |
3528095 | Billy (Angel) | https://en.wikipedia.org/w/index.php?title=Billy%20(Angel) | Billy (Angel)
im invokes John F. Kennedy Jr. who was a member of the family himself—but adamantly disliked the conduct of relatives. Dylan is aware that Angel is a vampire with a good potential to kill Billy but still invites him into the family compound. Kennedy also openly criticized relatives who were engaging in 'bad behavior'.
# Reception.
Stephanie Romanov says the ending to this episode was one of her "favorite Lilah moments. It was the only time Lilah was a hero."
DVD Verdict called this episode a "The Shining" homage with an "unsubtle metaphor" that "misogyny is BAD."
The Futon Critic named it the 36th best episode of 2001, saying "No show pushes as many buttons at the same time as this one." | 6,125,438 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
ICD-10 is an international statistical classification used in health care and related industries.
Produced by the World Health Organization, it is used in several countries around the world. Some have gone on to develop their own national enhancements, building off the international version of the classification.
Chapter XVII of ICD-10 deals with congenital malformations, deformations and chromosomal abnormalities; collectively known as birth defects. Examples of conditions captured using codes from Chapter XVII include; microcephaly, congenital absence of kidney, and Down syndrome.
# Q00–Q89 – Congenital | 6,125,439 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
malformations and deformations.
## (Q00–Q07) nervous system.
- () Anencephaly and similar malformations
- () Anencephaly
- Acephaly
- Acrania
- Amyelencephaly
- Hemianencephaly
- Hemicephaly
- () Craniorachischisis
- () Iniencephaly
- () Encephalocele
- () Microcephaly
- () Congenital hydrocephalus
- () Malformations of aqueduct of Sylvius
- () Atresia of foramina of Magendie and Luschka
- Dandy-Walker syndrome
- () Other congenital hydrocephalus
- () Congenital hydrocephalus, unspecified
- () Other congenital malformations of brain
- () Congenital malformations of corpus callosum
- () Arhinencephaly
- () Holoprosencephaly
- () Other reduction deformities of brain
- Agyria | 6,125,440 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
and Lissencephaly (EUROCAT Q04.33)
- Microgyria and Pachygyria (EUROCAT Q04.34)
- Hydranencephaly (EUROCAT Q04.35)
- () Septo-optic dysplasia
- () Megalencephaly
- () Congenital cerebral cysts
- Porencephaly
- Schizencephaly
- () Other specified congenital malformations of brain
- () Congenital malformation of brain, unspecified
- () Spina bifida
- hydromeningocele (spinal)
- meningocele(spinal)
- meningomyelocele
- myelocele
- myelomeningocele
- rachischisis
- syringomyelocele
- () Other congenital malformations of spinal cord
- () Amyelia
- () Hypoplasia and dysplasia of spinal cord
- () Diastematomyelia
- () Other congenital cauda equina malformations
- () Hydromyelia
- | 6,125,441 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
() Other specified congenital malformations of spinal cord
- () Congenital malformation of spinal cord, unspecified
- () Other congenital malformations of nervous system
- () Arnold-Chiari syndrome
- () Other specified congenital malformations of nervous system
- () Congenital malformation of nervous system, unspecified
## (Q10–Q18) eye, ear, face and neck.
### Eye.
- () Congenital malformations of eyelid, lacrimal apparatus and orbit
- () Congenital ptosis
- () Congenital ectropion
- () Congenital entropion
- () Other congenital malformations of eyelid
- Ablepharon
- Blepharophimosis, congenital
- Coloboma of eyelid
- () Absence and agenesis of lacrimal apparatus
- () Congenital | 6,125,442 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
stenosis and stricture of lacrimal duct
- () Other congenital malformations of lacrimal apparatus
- () Congenital malformation of orbit
- () Anophthalmos, microphthalmos and macrophthalmos
- () Cystic eyeball
- () Other anophthalmos
- () Microphthalmos
- () Macrophthalmos
- () Congenital lens malformations
- () Congenital cataract
- () Congenital displaced lens
- () Coloboma of lens
- () Congenital aphakia
- () Spherophakia
- () Other congenital lens malformations
- () Congenital lens malformation, unspecified
- () Congenital malformations of anterior segment of eye
- () Coloboma of iris
- () Absence of iris
- Aniridia
- () Other congenital malformations of iris
- () Congenital | 6,125,443 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
corneal opacity
- () Other congenital corneal malformations
- () Blue sclera
- () Other congenital malformations of anterior segment of eye
- () Congenital malformation of anterior segment of eye, unspecified
- () Congenital malformations of posterior segment of eye
- () Congenital malformation of vitreous humour
- () Congenital malformation of retina
- () Congenital malformation of optic disc
- Coloboma of optic disc
- () Congenital malformation of choroid
- () Other congenital malformations of posterior segment of eye
- Coloboma of the fundus
- () Congenital malformation of posterior segment of eye, unspecified
- () Other congenital malformations of eye
- () Congenital glaucoma
- | 6,125,444 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
Buphthalmos
- Glaucoma of newborn
- Hydrophthalmos
- Keratoglobus, congenital, with glaucoma
- Macrocornea with glaucoma
- Macrophthalmos in congenital glaucoma
- Megalocornea with glaucoma
### Ear.
- () Congenital malformations of ear causing impairment of hearing
- () Other congenital malformations of ear
- () Accessory auricle
- Accessory tragus
- Polyotia
- Preauricular appendage or tag
- () Macrotia
- () Microtia
- () Other misshapen ear
- Pointed ear
- () Misplaced ear
- Low-set ears
- () Prominent ear
- Bat ear
- () Other specified congenital malformations of ear
- () Congenital malformation of ear, unspecified
### Other face and neck.
- () Other congenital malformations | 6,125,445 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
of face and neck
- () Sinus, fistula and cyst of branchial cleft
- () Preauricular sinus and cyst
- () Other branchial cleft malformations
- Otocephaly
- () Webbing of neck
- () Macrostomia
- () Microstomia
- () Macrocheilia
- () Microcheilia
- () Other specified congenital malformations of face and neck
- () Congenital malformation of face and neck, unspecified
## (Q20–Q28) circulatory system.
- () Congenital malformations of cardiac chambers and connections
- () Common arterial trunk
- Persistent truncus arteriosus
- () Double outlet right ventricle
- Taussig-Bing syndrome
- () Double outlet left ventricle
- () Discordant ventriculoarterial connection
- Dextrotransposition | 6,125,446 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
of aorta
- Transposition of great vessels (complete)
- () Double inlet ventricle
- () Discordant atrioventricular connection
- Corrected transposition
- () Isomerism of atrial appendages
- () Congenital malformations of cardiac septa
- () Ventricular septal defect
- () Atrial septal defect
- () Atrioventricular septal defect
- Common atrioventricular canal
- Endocardial cushion defect
- Ostium primum atrial septal defect (type I)
- () Tetralogy of Fallot
- () Aortopulmonary septal defect
- Aortic septal defect
- Aortopulmonary window
- () Other congenital malformations of cardiac septa
- Eisenmenger's syndrome
- () Congenital malformations of pulmonary and tricuspid valves
- | 6,125,447 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
() Pulmonary valve atresia
- () Congenital pulmonary valve stenosis
- () Congenital pulmonary valve insufficiency
- () Other congenital malformations of pulmonary valve
- () Congenital tricuspid stenosis
- Tricuspid atresia
- () Ebstein's anomaly
- () Hypoplastic right heart syndrome
- () Other congenital malformations of tricuspid valve
- () Congenital malformation of tricuspid valve, unspecified
- () Congenital malformations of aortic and mitral valves
- () Congenital stenosis of aortic valve
- () Congenital insufficiency of aortic valve
- () Congenital mitral stenosis
- () Congenital mitral insufficiency
- () Hypoplastic left heart syndrome
- () Other congenital malformations | 6,125,448 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
of aortic and mitral valves
- () Congenital malformation of aortic and mitral valves, unspecified
- () Other congenital malformations of heart
- () Dextrocardia
- () Laevocardia
- () Cor triatriatum
- () Pulmonary infundibular stenosis
- () Congenital subaortic stenosis
- () Malformation of coronary vessels
- () Congenital heart block
- () Other specified congenital malformations of heart
- () Congenital malformation of heart, unspecified
- () Congenital malformations of great arteries
- () Patent ductus arteriosus
- () Coarctation of aorta
- () Atresia of aorta
- () Stenosis of aorta
- () Other congenital malformations of aorta
- Overriding aorta (EUROCAT Q25.42)
- Aneurysm | 6,125,449 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
of sinus of Valsalva (ruptured) (EUROCAT Q25.43)
- Double aortic arch (vascular ring of aorta)
- () Atresia of pulmonary artery
- () Stenosis of pulmonary artery
- () Other congenital malformations of pulmonary artery
- () Congenital malformations of great veins
- () Congenital stenosis of vena cava
- () Persistent left superior vena cava
- () Total anomalous pulmonary venous connection
- () Partial anomalous pulmonary venous connection
- () Anomalous pulmonary venous connection, unspecified
- () Anomalous portal venous connection
- () Portal vein-hepatic artery fistula
- () Other congenital malformations of great veins
- Scimitar syndrome
- () Congenital malformation of great | 6,125,450 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
vein, unspecified
- () Other congenital malformations of peripheral vascular system
- () Congenital absence and hypoplasia of umbilical artery
- () Congenital renal artery stenosis
- () Other congenital malformations of renal artery
- () Peripheral arteriovenous malformation
- () Congenital phlebectasia
- () Other specified congenital malformations of peripheral vascular system
- () Congenital malformation of peripheral vascular system, unspecified
- () Other congenital malformations of circulatory system
- () Arteriovenous malformation of precerebral vessels
- () Other malformations of precerebral vessels
- () Arteriovenous malformation of cerebral vessels
- () Other malformations | 6,125,451 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
of cerebral vessels
- () Other specified congenital malformations of circulatory system
- () Congenital malformation of circulatory system, unspecified
## (Q30–Q34) respiratory system.
- () Congenital malformations of nose
- () Choanal atresia
- () Agenesis and underdevelopment of nose
- () Fissured, notched and cleft nose
- () Congenital perforated nasal septum
- () Other congenital malformations of nose
- () Congenital malformation of nose, unspecified
- () Congenital malformations of larynx
- () Web of larynx
- () Congenital subglottic stenosis
- () Laryngeal hypoplasia
- () Laryngocele
- () Congenital laryngomalacia
- () Other congenital malformations of larynx
- () Congenital | 6,125,452 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
malformation of larynx, unspecified
- () Congenital malformations of trachea and bronchus
- () Congenital tracheomalacia
- () Other congenital malformations of trachea
- () Congenital bronchomalacia
- () Congenital stenosis of bronchus
- () Other congenital malformations of bronchus
- () Congenital malformations of lung
- () Congenital cystic lung
- () Accessory lobe of lung
- () Sequestration of lung
- () Agenesis of lung
- () Congenital bronchiectasis
- () Ectopic tissue in lung
- () Hypoplasia and dysplasia of lung
- () Other congenital malformations of lung
- () Congenital malformation of lung, unspecified
- () Other congenital malformations of respiratory system
- () Anomaly | 6,125,453 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
of pleura
- () Congenital cyst of mediastinum
- () Other specified congenital malformations of respiratory system
- () Congenital malformation of respiratory system, unspecified
## (Q35–Q45) digestive system.
- () Cleft palate
- () Cleft lip
- () Cleft palate with cleft lip
- () Other congenital malformations of tongue, mouth and pharynx
- () Congenital malformations of lips, not elsewhere classified
- Van der Woude's syndrome
- () Ankyloglossia
- () Macroglossia
- () Other congenital malformations of tongue
- Aglossia
- Bifid tongue
- Hypoplasia of tongue
- Hypoglossia
- Microglossia
- () Congenital malformations of salivary glands and ducts
- () Congenital malformations | 6,125,454 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
of palate, not elsewhere classified
- () Other congenital malformations of mouth
- () Pharyngeal pouch
- () Congenital malformations of oesophagus
- () Atresia of oesophagus without fistula
- () Atresia of oesophagus with tracheo-oesophageal fistula
- () Congenital tracheo-oesophageal fistula without atresia
- () Congenital stenosis and stricture of oesophagus
- () Oesophageal web
- () Congenital dilatation of oesophagus
- () Diverticulum of oesophagus
- () Other congenital malformations of oesophagus
- () Congenital malformation of oesophagus, unspecified
- () Other congenital malformations of upper alimentary tract
- () Congenital hypertrophic pyloric stenosis
- () Congenital | 6,125,455 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
hiatus hernia
- () Congenital absence, atresia and stenosis of small intestine
- () Congenital absence, atresia and stenosis of duodenum
- () Congenital absence, atresia and stenosis of jejunum
- () Congenital absence, atresia and stenosis of ileum
- () Congenital absence, atresia and stenosis of other specified parts of small intestine
- () Congenital absence, atresia and stenosis of small intestine, part unspecified
- () Congenital absence, atresia and stenosis of large intestine
- () Congenital absence, atresia and stenosis of rectum with fistula
- () Congenital absence, atresia and stenosis of rectum without fistula
- Imperforate rectum
- () Congenital absence, atresia and stenosis | 6,125,456 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
of anus with fistula
- () Congenital absence, atresia and stenosis of anus without fistula
- Imperforate anus
- () Congenital absence, atresia and stenosis of other parts of large intestine
- () Congenital absence, atresia and stenosis of large intestine, part unspecified
- () Other congenital malformations of intestine
- () Meckel's diverticulum
- () Hirschsprung's disease
- () Other congenital functional disorders of colon
- () Congenital malformations of intestinal fixation
- Malrotation of colon
- () Duplication of intestine
- () Ectopic anus
- () Congenital fistula of rectum and anus
- () Persistent cloaca
- () Other specified congenital malformations of intestine
- Dolichocolon
- | 6,125,457 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
Megaloappendix
- Megaloduodenum
- Microcolon
- () Congenital malformations of gallbladder, bile ducts and liver
- () Agenesis, aplasia and hypoplasia of gallbladder
- () Other congenital malformations of gallbladder
- () Atresia of bile ducts
- () Congenital stenosis and stricture of bile ducts
- () Choledochal cyst
- () Other congenital malformations of bile ducts
- () Cystic disease of liver
- () Other congenital malformations of liver
- Accessory liver
- Alagille's syndrome
- () Other congenital malformations of digestive system
- () Agenesis, aplasia and hypoplasia of pancreas
- () Annular pancreas
- () Congenital pancreatic cyst
- () Other congenital malformations of pancreas | 6,125,458 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
and pancreatic duct
- Accessory pancreas
- () Other specified congenital malformations of digestive system
- () Congenital malformation of digestive system, unspecified]]
## (Q50–Q56) genital organs.
- () Congenital malformations of ovaries, fallopian tubes and broad ligaments
- () Congenital malformations of uterus and cervix
- () Agenesis and aplasia of uterus
- () Doubling of uterus with doubling of cervix and vagina
- () Other doubling of uterus
- () Bicornate uterus
- () Unicornate uterus
- () Agenesis and aplasia of cervix
- () Embryonic cyst of cervix
- () Congenital fistulae between uterus and digestive and urinary tracts
- () Other congenital malformations of uterus and | 6,125,459 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
cervix
- () Congenital malformation of uterus and cervix, unspecified
- () Other congenital malformations of female genitalia
- () Congenital absence of vagina
- () Doubling of vagina
- () Congenital rectovaginal fistula
- () Imperforate hymen
- () Other congenital malformations of vagina
- () Fusion of labia
- () Congenital malformation of clitoris
- () Other congenital malformations of vulva
- () Other specified congenital malformations of female genitalia
- () Congenital malformation of female genitalia, unspecified
- () Undescended testicle
- () Hypospadias
- () Hypospadias, balanic
- () Hypospadias, penile
- () Hypospadias, penoscrotal
- () Hypospadias, perineal
- () | 6,125,460 |
3528104 | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities | https://en.wikipedia.org/w/index.php?title=ICD-10%20Chapter%20XVII:%20Congenital%20malformations,%20deformations%20and%20chromosomal%20abnormalities | ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
Congenital chordee
- () Other hypospadias
- () Hypospadias, unspecified
- () Other congenital malformations of male genital organs
- () Absence and aplasia of testis
- Monorchism
- () Hypoplasia of testis and scrotum
- () Other congenital malformations of testis and scrotum
- () Atresia of vas deferens
- () Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate
- () Congenital absence and aplasia of penis
- () Other congenital malformations of penis
- () Other specified congenital malformations of male genital organs
- () Congenital malformation of male genital organ, unspecified
- () Indeterminate sex and pseudohermaphroditism
- () Hermaphroditism, | 6,125,461 |
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not elsewhere classified
- () Male pseudohermaphroditism, not elsewhere classified
- () Female pseudohermaphroditism, not elsewhere classified
- () Pseudohermaphroditism, unspecified
- () Indeterminate sex, unspecified
## (Q60–Q64) urinary system.
- () Renal agenesis and other reduction defects of kidney
- () Renal agenesis, unilateral
- () Renal agenesis, bilateral
- () Renal agenesis, unspecified
- () Renal hypoplasia, unilateral
- () Renal hypoplasia, bilateral
- () Renal hypoplasia, unspecified
- () Potter sequence
- () Cystic kidney disease
- () Congenital single renal cyst
- () Polycystic kidney, autosomal recessive
- () Polycystic kidney, autosomal dominant
- () Polycystic | 6,125,462 |
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kidney, unspecified
- () Renal dysplasia
- () Medullary cystic kidney
- () Other cystic kidney diseases
- () Cystic kidney disease, unspecified
- Meckel-Gruber syndrome
- () Congenital obstructive defects of renal pelvis and congenital malformations of ureter
- () Congenital hydronephrosis
- () Atresia and stenosis of ureter
- () Congenital megaloureter
- () Other obstructive defects of renal pelvis and ureter
- () Agenesis of ureter
- () Duplication of ureter
- () Malposition of ureter
- () Congenital vesico-uretero-renal reflux
- () Other congenital malformations of ureter
- () Other congenital malformations of kidney
- () Accessory kidney
- () Lobulated, fused and horseshoe | 6,125,463 |
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kidney
- () Ectopic kidney
- () Hyperplastic and giant kidney
- () Other specified congenital malformations of kidney
- () Congenital malformation of kidney, unspecified
- () Other congenital malformations of urinary system
- () Epispadias
- () Exstrophy of urinary bladder
- () Congenital posterior urethral valves
- () Other atresia and stenosis of urethra and bladder neck
- () Malformation of urachus
- Cyst of urachus
- Patent urachus
- Prolapse of urachus
- () Congenital absence of bladder and urethra
- () Congenital diverticulum of bladder
- () Other congenital malformations of bladder and urethra
- () Other specified congenital malformations of urinary system
- () Congenital | 6,125,464 |
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malformation of urinary system, unspecified
## (Q65–Q79) musculoskeletal system.
- () Congenital deformities of hip
- () Congenital dislocation of hip, unilateral
- () Congenital dislocation of hip, bilateral
- () Congenital dislocation of hip, unspecified
- () Congenital subluxation of hip, unilateral
- () Congenital subluxation of hip, bilateral
- () Congenital subluxation of hip, unspecified
- () Unstable hip
- () Other congenital deformities of hip
- () Congenital deformity of hip, unspecified
- () Congenital deformities of feet
- () Talipes equinovarus
- () Talipes calcaneovarus
- () Metatarsus varus
- () Other congenital varus deformities of feet
- () Talipes calcaneovalgus
- | 6,125,465 |
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() Congenital pes planus
- () Other congenital valgus deformities of feet
- () Pes cavus
- () Other congenital deformities of feet
- () Congenital deformity of feet, unspecified
- () Congenital musculoskeletal deformities of head, face, spine and chest
- () Facial asymmetry
- () Compression facies
- () Dolichocephaly
- () Plagiocephaly
- () Other congenital deformities of skull, face and jaw
- () Congenital deformity of spine
- () Pectus excavatum
- () Pectus carinatum
- () Other congenital deformities of chest
- () Other congenital musculoskeletal deformities
- () Congenital deformity of sternocleidomastoid muscle
- () Congenital deformity of hand
- () Congenital deformity | 6,125,466 |
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of knee
- () Congenital bowing of femur
- () Congenital bowing of tibia and fibula
- () Congenital bowing of long bones of leg, unspecified
- () Other specified congenital musculoskeletal deformities
- () Polydactyly
- () Accessory finger(s)
- () Accessory thumb(s)
- () Accessory toe(s)
- () Polydactyly, unspecified
- () Syndactyly
- () Fused fingers
- () Webbed fingers
- () Fused toes
- () Webbed toes
- () Polysyndactyly
- () Syndactyly, unspecified
- () Reduction defects of upper limb
- () Congenital complete absence of upper limb(s)
- () Congenital absence of upper arm and forearm with hand present
- () Congenital absence of both forearm and hand
- () Congenital absence | 6,125,467 |
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of hand and finger(s)
- () Longitudinal reduction defect of radius
- () Longitudinal reduction defect of ulna
- () Lobster-claw hand
- () Other reduction defects of upper limb(s)
- () Reduction defect of upper limb, unspecified
- () Reduction defects of lower limb
- () Congenital complete absence of lower limb(s)
- () Congenital absence of thigh and lower leg with foot present
- () Congenital absence of both lower leg and foot
- () Congenital absence of foot and toe(s)
- () Longitudinal reduction defect of femur
- () Longitudinal reduction defect of tibia
- () Longitudinal reduction defect of fibula
- () Split foot
- () Other reduction defects of lower limb(s)
- () Reduction | 6,125,468 |
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defect of lower limb, unspecified
- () Reduction defects of unspecified limb
- () Congenital absence of unspecified limb(s)
- Amelia NOS
- () Phocomelia, unspecified limb(s)
- () Other reduction defects of unspecified limb(s)
- Ectromelia NOS
- Hemimelia NOS
- Reduction defect, NOS
- () Other congenital malformations of limb(s)
- () Other congenital malformations of upper limb(s), including shoulder girdle
- Accessory carpal bones
- Cleidocranial dysostosis
- Congenital pseudarthrosis of clavicle
- Macrodactylia (fingers)
- Madelung's deformity
- Radioulnar synostosis
- Sprengel's deformity
- Triphalangeal thumb
- () Congenital malformation of knee
- genu valgum
- genu varum
- | 6,125,469 |
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() Other congenital malformations of lower limb(s), including pelvic girdle
- () Arthrogryposis multiplex congenita
- () Other specified congenital malformations of limb(s)
- () Unspecified congenital malformation of limb(s)
- () Other congenital malformations of skull and face bones
- () Craniosynostosis
- Acrocephaly
- Imperfect fusion of skull
- Oxycephaly
- Trigonocephaly
- () Craniofacial dysostosis
- Crouzon's disease
- () Hypertelorism
- () Macrocephaly
- () Mandibulofacial dysostosis
- Franceschetti syndrome
- Treacher-Collins syndrome
- () Oculomandibular dysostosis
- () Other specified congenital malformations of skull and face bones
- Absence of skull bone, congenital
- | 6,125,470 |
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Congenital deformity of forehead
- Platybasia
- () Congenital malformation of skull and face bones, unspecified
- () Congenital malformations of spine and bony thorax
- () Spina bifida occulta
- () Klippel-Feil syndrome
- () Congenital spondylolisthesis
- () Congenital scoliosis due to congenital bony malformation
- () Other congenital malformations of spine, not associated with scoliosis
- () Cervical rib
- () Other congenital malformations of ribs
- () Congenital malformation of sternum
- Congenital absence of sternum
- Sternum bifidum
- () Other congenital malformations of bony thorax
- () Congenital malformation of bony thorax, unspecified
- () Osteochondrodysplasia with | 6,125,471 |
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defects of growth of tubular bones and spine
- () Achondrogenesis
- Hypochondrogenesis
- () Thanatophoric short stature
- () Short rib syndrome
- Asphyxiating thoracic dysplasia (Jeune)
- () Chondrodysplasia punctata
- () Achondroplasia
- Hypochondroplasia
- Osteosclerosis congenita
- () Diastrophic dysplasia
- () Chondroectodermal dysplasia
- Ellis-van Creveld syndrome
- () Spondyloepiphyseal dysplasia
- () Other osteochondrodysplasia with defects of growth of tubular bones and spine
- () Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified
- () Other osteochondrodysplasias
- () Osteogenesis imperfecta
- Fragilitas ossium
- Osteopsathyrosis
- | 6,125,472 |
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() Polyostotic fibrous dysplasia
- Albright(-McCune)(-Sternberg) syndrome
- () Osteopetrosis
- Albers-Schönberg syndrome
- () Progressive diaphyseal dysplasia
- Camurati-Engelmann syndrome
- () Enchondromatosis
- Maffucci's syndrome
- Ollier's disease
- () Metaphyseal dysplasia
- Pyle's syndrome
- () Multiple congenital exostoses
- Diaphyseal aclasis
- () Other specified osteochondrodysplasias
- Osteopoikilosis
- () Osteochondrodysplasia, unspecified
- Chondrodystrophy NOS
- Osteodystrophy NOS
- () Congenital malformations of the musculoskeletal system, not elsewhere classified
- () Congenital diaphragmatic hernia
- () Other congenital malformations of diaphragm
- () Exomphalos
- | 6,125,473 |
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Omphalocele
- () Gastroschisis
- () Prune belly syndrome
- () Other congenital malformations of abdominal wall
- () Ehlers-Danlos syndrome
- () Other congenital malformations of musculoskeletal system
- Accessory muscle
- Amyotrophia congenita
- Poland's syndrome
- () Congenital malformation of musculoskeletal system, unspecified
## (Q80–Q89) Other.
- () Congenital ichthyosis
- () Ichthyosis vulgaris
- () X-linked ichthyosis
- () Lamellar ichthyosis
- () Congenital bullous ichthyosiform erythroderma
- () Harlequin fetus
- () Other congenital ichthyosis
- () Congenital ichthyosis, unspecified
- () Epidermolysis bullosa
- () Epidermolysis bullosa simplex
- () Epidermolysis | 6,125,474 |
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bullosa letalis
- () Epidermolysis bullosa dystrophica
- () Other epidermolysis bullosa
- () Epidermolysis bullosa, unspecified
- () Other congenital malformations of skin
- () Hereditary lymphoedema
- () Xeroderma pigmentosum
- () Mastocytosis
- Urticaria pigmentosa
- () Incontinentia pigmenti
- () Ectodermal dysplasia (anhidrotic)
- () Congenital non-neoplastic naevus
- Birthmark NOS
- naevus flammeus / Port-wine stain
- sanguineous naevus
- strawberry naevus
- vascular naevus NOS
- verrucous naevus
- () Other specified congenital malformations of skin
- Abnormal palmar creases
- Accessory skin tags
- Benign familial pemphigus (Hailey-Hailey disease)
- Cutis laxa (hyperelastica)
- | 6,125,475 |
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Dermatoglyphic anomalies
- Inherited keratosis palmaris et plantaris
- Keratosis follicularis (Darier-White) (ILDS Q82.868)
- () Congenital malformation of skin, unspecified
- () Congenital malformations of breast
- () Congenital absence of breast with absent nipple
- () Accessory breast
- () Absent nipple
- () Accessory nipple
- Supernumerary nipple
- () Other congenital malformations of breast
- Hypoplasia of breast
- () Congenital malformation of breast, unspecified
- () Other congenital malformations of integument
- () Congenital alopecia
- () Congenital morphological disturbances of hair, not elsewhere classified
- Beaded hair
- Monilethrix
- Pili annulati
- Trichothiodystrophy | 6,125,476 |
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(ILDS Q84.169)
- () Other congenital malformations of hair
- () Anonychia
- () Congenital leukonychia
- () Enlarged and hypertrophic nails
- Congenital onychauxis
- Pachyonychia
- () Other congenital malformations of nails
- () Other specified congenital malformations of integument
- () Congenital malformation of integument, unspecified
- () Phakomatoses, not elsewhere classified
- () Neurofibromatosis (nonmalignant)
- Von Recklinghausen's disease (ILDS Q85.010)
- Neurofibromatosis II (ILDS Q85.020)
- Neurofibromatosis, segmental (ILDS Q85.030)
- () Tuberous sclerosis
- Bourneville's disease
- () Other phakomatoses, not elsewhere classified
- Sturge-Weber syndrome (EUROCAT | 6,125,477 |
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Q85.81)
- von Hippel-Lindau disease (EUROCAT Q85.82)
- () Phakomatosis, unspecified
- Hamartosis NOS
- () Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
- () Fetal alcohol syndrome (dysmorphic)
- () Fetal hydantoin syndrome
- Meadow's syndrome
- () Dysmorphism due to warfarin
- () Other congenital malformation syndromes due to known exogenous causes
- () Other specified congenital malformation syndromes affecting multiple systems
- () Congenital malformation syndromes predominantly affecting facial appearance
- Acrocephalopolysyndactyly
- Acrocephalosyndactyly (Apert)
- Cryptophthalmos syndrome
- Cyclopia
- Goldenhar syndrome
- Moebius | 6,125,478 |
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syndrome
- oro-facial-digital syndrome
- Robin syndrome
- Whistling face
- () Congenital malformation syndromes predominantly associated with short stature
- Aarskog syndrome
- Cockayne syndrome (ILDS Q87.110)
- De Lange syndrome (ILDS Q87.170)
- Dubowitz syndrome
- Noonan syndrome
- Prader-Willi syndrome
- Robinow-Silverman-Smith syndrome
- Silver-Russell syndrome (ILDS Q87.114)
- Seckel syndrome
- Smith-Lemli-Opitz syndrome
- Sjögren-Larsson syndrome (ILDS Q87.136)
- () Congenital malformation syndromes predominantly involving limbs
- Holt-Oram syndrome
- Klippel-Trénaunay-Weber (EUROCAT Q87.21, ILDS Q87.210)
- Nail-patella syndrome (ILDS Q87.230)
- Rubinstein-Taybi syndrome | 6,125,479 |
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(EUROCAT Q87.23)
- sirenomelia
- thrombocytopenia with absent radius syndrome
- VATER syndrome
- () Congenital malformation syndromes involving early overgrowth
- Beckwith-Wiedemann syndrome
- Sotos syndrome
- Weaver syndrome
- () Marfan's syndrome
- () Other congenital malformation syndromes with other skeletal changes
- () Other specified congenital malformation syndromes, not elsewhere classified
- Alport syndrome (EUROCAT Q87.80)
- Bardet-Biedl syndrome (EUROCAT Q87.81)
- Zellweger's syndrome (EUROCAT Q87.83)
- William's syndrome (EUROCAT Q87.84)
- Angelman's syndrome (Happy puppet syndrome) (EUROCAT Q87.85)
- Snyder–Robinson syndrome
- () Other congenital malformations, | 6,125,480 |
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not elsewhere classified
- () Congenital malformations of spleen
- Asplenia (congenital)
- Congenital splenomegaly
- () Congenital malformations of adrenal gland
- () Congenital malformations of other endocrine glands
- Congenital malformation of parathyroid or thyroid gland
- Persistent thyroglossal duct
- Thyroglossal cyst
- () Situs inversus
- () Conjoined twins
- () Multiple congenital malformations, not elsewhere classified
- () Other specified congenital malformations
- () Congenital malformation, unspecified
# Q90–Q99 – Chromosomal abnormalities, not elsewhere classified.
- () Down's syndrome
- () Trisomy 21, meiotic nondisjunction
- () Trisomy 21, mosaicism (mitotic | 6,125,481 |
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nondisjunction)
- () Trisomy 21, translocation
- () Down's syndrome, unspecified
- () Trisomy 18 and Trisomy 13
- () Trisomy 18, meiotic nondisjunction
- () Trisomy 18, mosaicism (mitotic nondisjunction)
- () Trisomy 18, translocation
- () Edwards' syndrome, unspecified
- () Trisomy 13, meiotic nondisjunction
- () Trisomy 13, mosaicism (mitotic nondisjunction)
- () Trisomy 13, translocation
- () Patau's syndrome, unspecified
- () Other trisomies and partial trisomies of the autosomes, not elsewhere classified
- Trisomy 9
- Warkany syndrome 2
- () Whole chromosome trisomy, meiotic nondisjunction
- () Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
- () Major partial | 6,125,482 |
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trisomy
- () Minor partial trisomy
- () Duplications seen only at prometaphase
- () Duplications with other complex rearrangements
- () Extra marker chromosomes
- () Triploidy and polyploidy
- () Other specified trisomies and partial trisomies of autosomes
- () Trisomy and partial trisomy of autosomes, unspecified
- () Monosomies and deletions from the autosomes, not elsewhere classified
- () Whole chromosome monosomy, meiotic nondisjunction
- () Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
- () Chromosome replaced with ring or dicentric
- () Deletion of short arm of chromosome 4
- Wolff-Hirschorn syndrome
- () Deletion of short arm of chromosome 5
- Cri-du-chat | 6,125,483 |
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syndrome
- () Other deletions of part of a chromosome
- Angelman syndrome
- () Deletion seen only at prometaphase
- () Deletions with other complex rearrangements
- () Other deletions from the autosomes
- () Deletion from autosomes, unspecified
- () Balanced rearrangements and structural markers, not elsewhere classified
- Robertsonian and balanced reciprocal translocations and insertions
- () Balanced translocation and insertion in normal individual
- () Chromosome inversion in normal individual
- () Balanced autosomal rearrangement in abnormal individual
- () Balanced sex/autosomal rearrangement in abnormal individual
- () Individuals with marker heterochromatin
- () Individuals | 6,125,484 |
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with autosomal fragile site
- () Other balanced rearrangements and structural markers
- () Balanced rearrangement and structural marker, unspecified
- () Turner syndrome
- () Karyotype 45,X
- () Karyotype 46,X iso (Xq)
- () Karyotype 46,X with abnormal sex chromosome, except iso (Xq)
- () Mosaicism, 45,X/46,XX or XY
- () Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome
- () Other variants of Turner's syndrome
- () Turner's syndrome, unspecified
- () Other sex chromosome abnormalities, female phenotype, not elsewhere classified
- () Karyotype 47,XXX
- () Female with more than three X chromosomes
- () Mosaicism, lines with various numbers of X chromosomes
- () Female | 6,125,485 |
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with 46,XY karyotype
- () Other specified sex chromosome abnormalities, female phenotype
- () Sex chromosome abnormality, female phenotype, unspecified
- () Other sex chromosome abnormalities, male phenotype, not elsewhere classified
- () Klinefelter's syndrome karyotype 47,XXY
- () Klinefelter's syndrome, male with more than two X chromosomes
- () Klinefelter's syndrome, male with 46,XX karyotype
- () Other male with 46,XX karyotype – XX male syndrome
- () Klinefelter's syndrome, unspecified
- () Karyotype 47,XYY
- () Male with structurally abnormal sex chromosome
- () Male with sex chromosome mosaicism
- () Other specified sex chromosome abnormalities, male phenotype
- () Sex | 6,125,486 |
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ale with sex chromosome mosaicism
- () Other specified sex chromosome abnormalities, male phenotype
- () Sex chromosome abnormality, male phenotype, unspecified
- () Other chromosome abnormalities, not elsewhere classified
- () Chimera 46,XX/46,XY
- () 46,XX true hermaphrodite
- 46,XX with streak gonads
- 46,XY with streak gonads
- Pure gonadal dysgenesis
- () Fragile X chromosome
- Fragile X syndrome
- () Other specified chromosome abnormalities
- () Chromosomal abnormality, unspecified
# Excludes.
Inborn errors of metabolism (E70-E88)
# See also.
- List of ICD-10 codes
- International Statistical Classification of Diseases and Related Health Problems
- Congenital disorder | 6,125,487 |
3528112 | William Arnold Carter | https://en.wikipedia.org/w/index.php?title=William%20Arnold%20Carter | William Arnold Carter
William Arnold Carter
William Arnold Carter (June 27, 1907 – May 18, 1996) was the Governor of the Panama Canal Zone from 1960 to 1962.
# Biography.
He was born in Corsicana, Texas on June 27, 1907 to William Arnold Carter and Susan Young.
He graduated from the United States Military Academy at West Point in 1930. In 1933 he earned a B.S. in civil engineering from University of California. His World War II service included being chief engineer of the II Corps in the Mediterranean, and chief engineer of the 1st Army during the Normandy Invasion and European Campaign. He served as Panama Canal Zone Governor from 1960 to 1962.
He died on May 18, 1996 in Washington, D.C. | 6,125,488 |
3528114 | Oh, What a Night (1992 film) | https://en.wikipedia.org/w/index.php?title=Oh,%20What%20a%20Night%20(1992%20film) | Oh, What a Night (1992 film)
Oh, What a Night (1992 film)
Oh, What a Night is a 1992 comedy film, starring Corey Haim and Barbara Williams.
# Plot summary.
Two teenage boys are growing up in a small Canadian town in the summer of 1955. While their parents go about with their own concerns, the two develop an interest in girls. One tries to impress his crush with his father’s cars. The other, seventeen-year-old Eric Hansen (Corey Haim), becomes enamored with an older woman newly arrived in town.
# Cast.
- Corey Haim ... Eric
- Barbara Williams ... Vera
- Keir Dullea ... Thorvald
- Emilie-Claire Barlow ... Lorraine
- Geneviève Bujold ... Eva
- Andrew Miller ... Donald
- Kirsten Kieferle ... Betty
- Joseph Ziegler | 6,125,489 |
3528114 | Oh, What a Night (1992 film) | https://en.wikipedia.org/w/index.php?title=Oh,%20What%20a%20Night%20(1992%20film) | Oh, What a Night (1992 film)
ring Corey Haim and Barbara Williams.
# Plot summary.
Two teenage boys are growing up in a small Canadian town in the summer of 1955. While their parents go about with their own concerns, the two develop an interest in girls. One tries to impress his crush with his father’s cars. The other, seventeen-year-old Eric Hansen (Corey Haim), becomes enamored with an older woman newly arrived in town.
# Cast.
- Corey Haim ... Eric
- Barbara Williams ... Vera
- Keir Dullea ... Thorvald
- Emilie-Claire Barlow ... Lorraine
- Geneviève Bujold ... Eva
- Andrew Miller ... Donald
- Kirsten Kieferle ... Betty
- Joseph Ziegler ... Vern Rawlins
- Robbie Coltrane ... Todd
- Denny Doherty ... Harol | 6,125,490 |
3528069 | Arthur Benjamin | https://en.wikipedia.org/w/index.php?title=Arthur%20Benjamin | Arthur Benjamin
Arthur Benjamin
Arthur Leslie Benjamin (Sydney, 18 September 1893London, 10 April 1960) was an Australian composer, pianist, conductor and teacher. He is best known as the composer of "Jamaican Rumba" (1938), the "Storm Clouds Cantata" featured in both versions of the Alfred Hitchcock film "The Man who Knew Too Much" (1934), (1956).
# Biography.
Arthur Benjamin was born in Sydney on 18 September 1893 into a Jewish family, although he was a non-practicing Jew. His parents moved to Brisbane when Arthur was three years old. At the age of six, he made his first public appearance as a pianist and his formal musical training began three years later with George Sampson, the Organist of St John's | 6,125,491 |
3528069 | Arthur Benjamin | https://en.wikipedia.org/w/index.php?title=Arthur%20Benjamin | Arthur Benjamin
Cathedral and Brisbane City Organist. In 1911, Benjamin won a scholarship from Brisbane Grammar School to the Royal College of Music (RCM), where he studied composition with Charles Villiers Stanford, harmony and counterpoint with Thomas Dunhill, and piano with Frederic Cliffe.
In 1914 he joined the Officer Training Corps, receiving a temporary commission in April 1915. He served initially in the infantry as 2nd Lieutenant with the 32nd Battalion of the Royal Fusiliers and in November 1917 he was attached to the Royal Flying Corps. On 31 July 1918 his aircraft was shot down over Germany by the young Hermann Göring, and he spent the remainder of the war as a German prisoner of war at Ruhleben | 6,125,492 |
3528069 | Arthur Benjamin | https://en.wikipedia.org/w/index.php?title=Arthur%20Benjamin | Arthur Benjamin
internment camp near Berlin. There he met the composer Edgar Bainton, who had been interned since 1914, and who was later to become director of the New South Wales State Conservatorium of Music.
The manuscript of the unpublished Violin Sonata in E minor bears the date 1918, the only surviving work of that year and one of very few to be written by Benjamin during the war.
He returned to Australia in 1919 and became piano professor at the NSW State Conservatorium of Music, Sydney. He returned to England in 1921 to become piano professor at the RCM. Following his appointment in 1926 to a professorship which he held for the next thirteen years at the RCM, Benjamin developed a distinguished career | 6,125,493 |
3528069 | Arthur Benjamin | https://en.wikipedia.org/w/index.php?title=Arthur%20Benjamin | Arthur Benjamin
as a piano teacher. His better-known students from that era include Muir Mathieson, Peggy Glanville-Hicks, Miriam Hyde, Joan Trimble, Stanley Bate, Bernard Stevens, Lamar Crowson, Alun Hoddinott, Dorian Le Gallienne, Natasha Litvin (later Stephen Spender's wife and a prominent concert pianist), William Blezard and Benjamin Britten, whose "Holiday Diary" suite for solo piano is dedicated to Benjamin and mimics many of his teacher's mannerisms.
He continued writing chamber works for the next few years – Three Pieces for violin and piano (1919–24); "Three Impressions" (voice and string quartet, 1919); "Five Pieces for Cello" (1923); "Pastoral Fantasy" (string quartet, 1924), which won a Carnegie | 6,125,494 |
3528069 | Arthur Benjamin | https://en.wikipedia.org/w/index.php?title=Arthur%20Benjamin | Arthur Benjamin
Award that year; Sonatina (violin and piano, 1924).
Orchestral works became more common after 1927 – "Rhapsody on Negro Themes" (MS 1919); Concertino for piano and orchestra (1926/7); "Light Music Suite" (1928); "Overture to an Italian Comedy" (1937); "Cotillon" Suite (1938). There also appeared over twenty meticulously crafted songs and choral settings.
He was also an adjudicator and examiner for the Associated Board of the Royal Schools of Music, which led him to places such as Australia, Canada and the West Indies. It was in the West Indies that he discovered the native tune ("Mango Walk") on which he based his best-known piece, "Jamaican Rumba", one of "Two Jamaican Pieces", composed in | 6,125,495 |
3528069 | Arthur Benjamin | https://en.wikipedia.org/w/index.php?title=Arthur%20Benjamin | Arthur Benjamin
1938, for which the Jamaican government gave him a free barrel of rum a year as thanks for making their country known.
The Violin Concerto of 1932 was premiered by Antonio Brosa with Benjamin conducting the BBC Symphony Orchestra. In 1935 he accompanied the 10-year-old Canadian cellist Lorne Munroe on a concert tour of Europe. Three years later he wrote a Sonatina for Munroe, who later became the principal cellist with the Philadelphia Orchestra and the New York Philharmonic, and also recorded the piece.
His "Romantic Fantasy for Violin, Viola and Orchestra" was premiered by Eda Kersey and Bernard Shore in 1938, under the composer. Its first recording was by Jascha Heifetz and William Primrose.
He | 6,125,496 |
3528069 | Arthur Benjamin | https://en.wikipedia.org/w/index.php?title=Arthur%20Benjamin | Arthur Benjamin
resigned from his post at the RCM and left to settle in Vancouver, British Columbia, Canada, where he remained for the duration of the war. In 1941 he was appointed conductor of the newly formed CBC Symphony Orchestra, holding the post until 1946. During this time he gave "literally hundreds" of Canadian first performances. After a series of radio talks and concerts in addition to music teaching, conducting and composing, he became a major figure in Canadian musical life. He frequently visited the United States, broadcasting and arranging many performances of contemporary British music. He was also Resident Lecturer at Reed College, Portland, Oregon between 1944 and 1945. Notable students include | 6,125,497 |
3528069 | Arthur Benjamin | https://en.wikipedia.org/w/index.php?title=Arthur%20Benjamin | Arthur Benjamin
composer Pamela Harrison.
The "Elegiac Mazurka" of 1941 was commissioned as part of the memorial volume 'Homage to Paderewski' in honour of the Polish pianist who had died that year. In 1945 a shortened piano solo arrangement of the "Jamaican Rumba" was published.
The other major original works written during the 1950s were the Harmonica Concerto (1953), written for Larry Adler, who performed it many times and recorded it at least twice; the ballet "Orlando's Silver Wedding" (1951), "Tombeau de Ravel" for clarinet and piano, a second string quartet (1959) and the Wind Quintet (1960). He had a lasting admiration for Maurice Ravel, whose influence is most obvious in "Tombeau de Ravel" and the | 6,125,498 |
3528069 | Arthur Benjamin | https://en.wikipedia.org/w/index.php?title=Arthur%20Benjamin | Arthur Benjamin
much earlier Suite of 1926 for piano solo.
He was honoured by the Worshipful Company of Musicians by the award of the Cobbett Medal later that year (1957).
His private students included John Carmichael.
Arthur Benjamin died on 10 April 1960, at the age of 66, at the Middlesex Hospital, London, from a re-occurrence of the cancer that had first attacked him three years earlier. An alternative explanation of the immediate cause of death is hepatitis, contracted while Benjamin and his partner, Jack Henderson, a Canadian who worked in the music publishing business, were holidaying with the Australian painter Donald Friend in Ceylon (now Sri Lanka).
## Operas.
Benjamin wrote four operas. The | 6,125,499 |
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