OMOP Concept 4291019
Disorder of tyrosine metabolism
StandardConditionSNOMED37200009Disorder
Maps from
15
Descendants
25
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
15 source codes normalize to Disorder of tyrosine metabolism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141858 | Disturbance of tyrosine metabolism | Non-standard |
| CIM10 | E70.2 | Disorders of tyrosine metabolism | Non-standard |
| ICD10 | E70.2 | Disorders of tyrosine metabolism | Non-standard |
| ICD10CM | E70.2 | Disorders of tyrosine metabolism | Non-standard |
| ICD10CM | E70.20 | Disorder of tyrosine metabolism, unspecified | Non-standard |
| ICD10CM | E70.29 | Other disorders of tyrosine metabolism | Non-standard |
| ICD10CN | E70.2 | Disorders of tyrosine metabolism | Non-standard |
| ICD10CN | E70.200 | Disorders of tyrosine metabolism | Non-standard |
| ICD10CN | E70.201 | High tyrosinemia (machine translation) | Non-standard |
| ICD10CN | E70.202 | Black uric acid disease (machine translation) | Non-standard |
| ICD10CN | E70.203 | Brown yellow disease (machine translation) | Non-standard |
| ICD10CN | E70.204 | Tyrosine aciduria (machine translation) | Non-standard |
| ICD10GM | E70.2 | Disorders of tyrosine metabolism | Non-standard |
| KCD7 | E70.2 | Disorders of tyrosine metabolism | Non-standard |
| Nebraska Lexicon | 37200009 | Disturbance of tyrosine metabolism | Non-standard |
Synonyms
Alternative names recorded for Disorder of tyrosine metabolism across source vocabularies.
- Disorder of tyrosine metabolism (disorder)
- Disturbance of tyrosine metabolism
- trastorno del metabolismo de la tirosina
- trastorno del metabolismo de la tirosina (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(6)Roll up to these when you need a wider cohort.
Narrower concepts
(25)Included automatically when you query with descendants.
- 14-Hydroxyphenylpyruvate dioxygenase deficiency
- 1Disorder of catecholamine synthesis
- 1Hepatic tyrosine aminotransferase deficiency
- 1Homogentisate 1,2-dioxygenase deficiency
- 1Hypertyrosinemia
- 1Hypopigmentation-immunodeficiency disease
- 1Tyrosinase-negative oculocutaneous albinism
- 1Tyrosinemia
- 1Tyrosinosis
- 1Tyrosinuria
- 1Woolf's syndrome
- 2Aromatic amino acid decarboxylase deficiency
- 2Dopamine beta-hydroxylase deficiency
- 2Fumarylacetoacetase deficiency, chronic type
- 2Griscelli syndrome type 1
- 2Griscelli syndrome type 3
- 2Hawkinsinuria
- 2Hereditary hypertyrosinemia
- 2Minimal pigment oculocutaneous albinism
- 2Temperature-sensitive oculocutaneous albinism
- 2Transient neonatal hypertyrosinemia
- 2Tyrosinemia type III
- 2Yellow mutant oculocutaneous albinism
- 3Tyrosinemia type 1
- 3Tyrosinemia type 2
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