icd10Code
stringlengths 5
8
| Disease
stringlengths 4
228
|
|---|---|
E67.8
|
Other specified hyperalimentation
|
E70.0
|
Classical phenylketonuria
|
E70.1
|
Other hyperphenylalaninemias
|
E70.2
|
Disorders of tyrosine metabolism
|
E70.20
|
Disorder of tyrosine metabolism unspecified
|
E70.21
|
Tyrosinemia
|
E70.29
|
Other disorders of tyrosine metabolism
|
E70.3
|
Albinism
|
E70.30
|
Albinism unspecified
|
E70.31
|
Ocular albinism
|
E70.310
|
X-linked ocular albinism
|
E70.311
|
Autosomal recessive ocular albinism
|
E70.318
|
Other ocular albinism
|
E70.319
|
Ocular albinism unspecified
|
E70.32
|
Oculocutaneous albinism
|
E70.320
|
Tyrosinase negative oculocutaneous albinism
|
E70.321
|
Tyrosinase positive oculocutaneous albinism
|
E70.328
|
Other oculocutaneous albinism
|
E70.329
|
Oculocutaneous albinism unspecified
|
E70.33
|
Albinism with hematologic abnormality
|
E70.330
|
Chediak-Higashi syndrome
|
E70.331
|
Hermansky-Pudlak syndrome
|
E70.338
|
Other albinism with hematologic abnormality
|
E70.339
|
Albinism with hematologic abnormality unspecified
|
E70.39
|
Other specified albinism
|
E70.4
|
Disorders of histidine metabolism
|
E70.40
|
Disorders of histidine metabolism unspecified
|
E70.41
|
Histidinemia
|
E70.49
|
Other disorders of histidine metabolism
|
E70.5
|
Disorders of tryptophan metabolism
|
E70.8
|
Other disorders of aromatic amino-acid metabolism
|
E70.9
|
Disorder of aromatic amino-acid metabolism unspecified
|
E71.0
|
Maple-syrup-urine disease
|
E71.1
|
Other disorders of branched-chain amino-acid metabolism
|
E71.11
|
Branched-chain organic acidurias
|
E71.110
|
Isovaleric acidemia
|
E71.111
|
3-methylglutaconic aciduria
|
E71.118
|
Other branched-chain organic acidurias
|
E71.12
|
Disorders of propionate metabolism
|
E71.120
|
Methylmalonic acidemia
|
E71.121
|
Propionic acidemia
|
E71.128
|
Other disorders of propionate metabolism
|
E71.19
|
Other disorders of branched-chain amino-acid metabolism
|
E71.2
|
Disorder of branched-chain amino-acid metabolism unspecified
|
E71.3
|
Disorders of fatty-acid metabolism
|
E71.30
|
Disorder of fatty-acid metabolism unspecified
|
E71.31
|
Disorders of fatty-acid oxidation
|
E71.310
|
Long chain/very long chain acyl CoA dehydrogenase deficiency
|
E71.311
|
Medium chain acyl CoA dehydrogenase deficiency
|
E71.312
|
Short chain acyl CoA dehydrogenase deficiency
|
E71.313
|
Glutaric aciduria type II
|
E71.314
|
Muscle carnitine palmitoyltransferase deficiency
|
E71.318
|
Other disorders of fatty-acid oxidation
|
E71.32
|
Disorders of ketone metabolism
|
E71.39
|
Other disorders of fatty-acid metabolism
|
E71.4
|
Disorders of carnitine metabolism
|
E71.40
|
Disorder of carnitine metabolism unspecified
|
E71.41
|
Primary carnitine deficiency
|
E71.42
|
Carnitine deficiency due to inborn errors of metabolism
|
E71.43
|
Iatrogenic carnitine deficiency
|
E71.44
|
Other secondary carnitine deficiency
|
E71.440
|
Ruvalcaba-Myhre-Smith syndrome
|
E71.448
|
Other secondary carnitine deficiency
|
E71.5
|
Peroxisomal disorders
|
E71.50
|
Peroxisomal disorder unspecified
|
E71.51
|
Disorders of peroxisome biogenesis
|
E71.510
|
Zellweger syndrome
|
E71.511
|
Neonatal adrenoleukodystrophy
|
E71.518
|
Other disorders of peroxisome biogenesis
|
E71.52
|
X-linked adrenoleukodystrophy
|
E71.520
|
Childhood cerebral X-linked adrenoleukodystrophy
|
E71.521
|
Adolescent X-linked adrenoleukodystrophy
|
E71.522
|
Adrenomyeloneuropathy
|
E71.528
|
Other X-linked adrenoleukodystrophy
|
E71.529
|
X-linked adrenoleukodystrophy unspecified type
|
E71.53
|
Other group 2 peroxisomal disorders
|
E71.54
|
Other peroxisomal disorders
|
E71.540
|
Rhizomelic chondrodysplasia punctata
|
E71.541
|
Zellweger-like syndrome
|
E71.542
|
Other group 3 peroxisomal disorders
|
E71.548
|
Other peroxisomal disorders
|
E72.0
|
Disorders of amino-acid transport
|
E72.00
|
Disorders of amino-acid transport unspecified
|
E72.01
|
Cystinuria
|
E72.02
|
Hartnup's disease
|
E72.03
|
Lowe's syndrome
|
E72.04
|
Cystinosis
|
E72.09
|
Other disorders of amino-acid transport
|
E72.1
|
Disorders of sulfur-bearing amino-acid metabolism
|
E72.10
|
Disorders of sulfur-bearing amino-acid metabolism unspecified
|
E72.11
|
Homocystinuria
|
E72.12
|
Methylenetetrahydrofolate reductase deficiency
|
E72.19
|
Other disorders of sulfur-bearing amino-acid metabolism
|
E72.2
|
Disorders of urea cycle metabolism
|
E72.20
|
Disorder of urea cycle metabolism unspecified
|
E72.21
|
Argininemia
|
E72.22
|
Arginosuccinic aciduria
|
E72.23
|
Citrullinemia
|
E72.29
|
Other disorders of urea cycle metabolism
|
E72.3
|
Disorders of lysine and hydroxylysine metabolism
|
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