CUI string | AUI string | ATUI string | SATUI string | SAB string | DEF string | SUPPRESS string | CVF null |
|---|---|---|---|---|---|---|---|
C5975713 | A7600061 | AT198017494 | null | NCI | A laboratory finding indicating decreased number of hematopoietic cells in the bone marrow. It may result from decreased proliferation of all or part of the hematopoietic series (erythroid, myeloid, and megakaryocytic). Microscopically, the hematopoietic cells are replaced by adipocytes. | N | null |
C5975716 | A7635882 | AT279858566 | null | NCI | A lymphoproliferative disorder composed of neoplastic B-cells. It includes B-cell non-Hodgkin lymphomas, B-cell leukemias, plasma cell neoplasms, and B-cell proliferations of uncertain malignant potential. | N | null |
C5975717 | A34645590 | AT277513607 | null | ORPHANET | NDE1-related microhydranencephaly is a rare, hereditary syndrome with a central nervous system malformation as major feature characterized by extreme microcephaly and growth restriction, severe motor delay and mental retardation, and typical radiological findings of gross dilation of the ventricles resulting from the a... | N | null |
C5975717 | A35236566 | AT283641988 | 5099328016 | SNOMEDCT_US | A rare hereditary syndrome with characteristics of extreme microcephaly and growth restriction, severe motor delay, intellectual disability and typical radiological findings of gross dilation of the ventricles resulting from the absence (or severe delay in the development) of cerebral hemispheres, hypoplasia of the cor... | O | null |
C5975717 | A35236566 | AT302971925 | 5400285010 | SNOMEDCT_US | NDE1-related microhydranencephaly is a rare, hereditary syndrome with a central nervous system malformation as major feature characterized by extreme microcephaly and growth restriction, severe motor delay and mental retardation, and typical radiological findings of gross dilation of the ventricles resulting from the a... | N | null |
C5975717 | A35236566 | AT302987855 | 5400286011 | SNOMEDCT_US | NDE1-related microhydranencephaly is a rare, hereditary syndrome with a central nervous system malformation as major feature characterised by extreme microcephaly and growth restriction, severe motor delay and mental retardation, and typical radiological findings of gross dilation of the ventricles resulting from the a... | N | null |
C5975717 | A35548313 | AT287993527 | 2815991000209111 | SCTSPA | Es un síndrome hereditario poco frecuente, que tiene como rasgo principal una microcefalia extrema y restricción del crecimiento y retraso psicomotor e intelectual grave, así como hallazgos radiológicos típicos, como gran dilatación de los ventrículos derivada de la ausencia (o retraso grave del desarrollo) de los hemi... | N | null |
C5978143 | A37216505 | AT305121743 | null | LNC | CDC - NHSN | N | null |
C5978144 | A37230896 | AT305103186 | null | LNC | Recurrence Score (RS) ranging from 0-100 | N | null |
C5978145 | A37225388 | AT305121754 | null | LNC | Recurrence Score (RS) ranging from 0-100 | N | null |
C5978146 | A37221413 | AT305125460 | null | LNC | Recurrence Score (RS) ranging from 0-100 | N | null |
C5978147 | A37223681 | AT305114198 | null | LNC | Recurrence Score (RS) ranging from 0-100 | N | null |
C5978148 | A37223682 | AT305106805 | null | LNC | Recurrence Score (RS) ranging from 0-100 | N | null |
C5978149 | A37228200 | AT305110562 | null | LNC | Recurrence Score (RS) ranging from 0-100 | N | null |
C5978273 | A37235041 | AT305180301 | 1703411000124111 | SNOMEDCT_US | Medication list that are private and need patient consent to share are medications that are used for substance abuse. | N | null |
C5978292 | A37234642 | AT305307110 | 1763541000124112 | SNOMEDCT_US | The organizational identifier assigned to the person who collected the specimen (i.e. collector) is missing or unreadable on the specimen container label. | N | null |
C5978309 | A37234632 | AT305611562 | 1764911000124117 | SNOMEDCT_US | The state of one's physical appearance or behaviors that do not align with societal expectations for a given gender. (a feminine boy, a masculine girl, etc.).. | N | null |
C5978346 | A37234549 | AT305357689 | 1824171000124119 | SNOMEDCT_US | Regular continuous, defined as the intent to treat for 52 weeks/year and receiving a minimum of an a priori defined frequency of infusions for at least 45 weeks (85%) of the year under consideration, replacement therapy started in the absence of documented joint disease, determined by physical examination and/or imagin... | N | null |
C5978347 | A37234744 | AT305357690 | 1824211000124117 | SNOMEDCT_US | Regular continuous, defined as the intent to treat for 52 weeks/year and receiving a minimum of an a priori defined frequency of infusions for at least 45 weeks (85%) of the year under consideration, replacement therapy started after two or more joint bleeds but before the onset of joint disease documented by physical ... | N | null |
C5978348 | A37234209 | AT305712267 | 1824221000124113 | SNOMEDCT_US | Regular continuous, defined as the intent to treat for 52 weeks/year and receiving a minimum of an a priori defined frequency of infusions for at least 45 weeks (85%) of the year under consideration, replacement therapy started after the onset of joint disease documented by physical examination and plain radiographs of... | N | null |
C5978369 | A24103569 | AT206839447 | null | LNC | Word pronounced incorrectly | N | null |
C5978369 | A24103569 | AT252649674 | null | LNC | (J0400=1 thru 4) | N | null |
C5978369 | A24103569 | AT285784490 | null | LNC | The patient has not fallen previously either at home or while hospitalized within the past 3 months. | N | null |
C5978374 | A37239114 | AT305942752 | null | MSHPOR | Emprego da força para fazer movimento de forma contínua para trabalhar somente o músculo desejado. | N | null |
C5978378 | A37241965 | AT305944322 | null | MSHPOR | Transmissão de patógenos do animal para o ser humano. | N | null |
C5978389 | A37236379 | AT305944320 | null | MSHPOR | Arte marcial de ataque e defesa introduzida no Brasil por escravizados Bantos e atualmente praticada como jogo e esporte. (Adaptado de Dicionário Houaiss) | N | null |
C5978390 | A37236147 | AT305942755 | null | MSHPOR | Antecipação da morte fora do tempo natural ou esperado, devido a fatores econômico-sociais, como: classe social, pobreza, violência, chacinas, drogas, bem como em decorrência da falta de condições de dignidade. (https://periodicorease.pro.br/rease/article/view/13396/6484) | N | null |
C5978390 | A37237994 | AT305944545 | null | MSHSPA | Anticipación de la muerte fuera del tiempo natural o esperado, por factores económico-sociales, tales como: clase social, pobreza, violencia, masacres, drogas, así como por la falta de condiciones de dignidad. (Tradución libre de: https://periodicorease.pro.br/rease/article/view/13396/6484) | N | null |
C5978398 | A37236767 | AT305941035 | null | MSHSPA | Rama de la zoología de invertebrados que se ocupa del estudio de los moluscos. | N | null |
C5978398 | A37241771 | AT305942394 | null | MSHPOR | Ramo da zoologia de invertebrados envolvida no estudo dos moluscos. | N | null |
C5979805 | A36931601 | AT301947512 | null | NCI | A healthcare facility in which patients are provided routine urgent and non-urgent care. | N | null |
C5979806 | A36942796 | AT301938627 | null | NCI | A neuroblastoma that has spread to the spinal canal. It may result in spinal cord compression. | N | null |
C5979810 | A24360516 | AT205729858 | null | NCI | Loss of movement function. | N | null |
C5979821 | A34640313 | AT277512822 | null | ORPHANET | Pure hair and nail ectodermal dysplasia is characterised by the association of onychodystrophy and severe hypotrichosis, which is mainly limited to the scalp but may also affect the eyelashes and eyebrows. Less than 20 cases have been reported so far. The mode of transmission is autosomal dominant. | N | null |
C5979867 | A2971969 | AT195389090 | 2884790012 | SNOMEDCT_US | Tumor-like mass in lungs composed of fibrous tissue or granulation tissue with inflammatory cells | O | null |
C5979867 | A2971969 | AT253581224 | 3777355015 | SNOMEDCT_US | Tumor-like mass in lungs composed of fibrous tissue or granulation tissue with inflammatory cells. | N | null |
C5979867 | A2971969 | AT253908822 | 3777356019 | SNOMEDCT_US | Tumour-like mass in lungs composed of fibrous tissue or granulation tissue with inflammatory cells. | N | null |
C5979867 | A6185597 | AT194176430 | 2919679015 | SCTSPA | Masa semejante a un tumor en los pulmones constituida por tejido fibroso o de granulación con células inflamatorias | O | null |
C5979867 | A6185597 | AT256448235 | 1805341000209116 | SCTSPA | Masa semejante a un tumor en los pulmones constituida por tejido fibroso o de granulación con células inflamatorias. | N | null |
C5979868 | A31611547 | AT274515468 | null | NCI | An autosomal dominant subtype of dilated cardiomyopathy caused by mutation(s) in the LMNA gene, encoding lamin-A and lamin C. | N | null |
C5979869 | A35657908 | AT288955951 | null | HPO | Applies to a sign or symptom that is provoked or brought about by administration of a medication. [] | N | null |
C5979870 | A36776135 | AT304905803 | null | HPO | An anomaly in demeanor, which refers to the outward behavior, manner, or conduct of a person. It encompasses how an individual presents themselves to others in terms of attitude, posture, and general comportment. [] | N | null |
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