OMOP Concept 4035264
Minimal pigment oculocutaneous albinism
StandardConditionSNOMED237919007Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Minimal pigment oculocutaneous albinism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 237919007 | Minimal pigment oculocutaneous albinism | Non-standard |
Synonyms
Alternative names recorded for Minimal pigment oculocutaneous albinism across source vocabularies.
- albinismo oculocutáneo pigmentario mínimo
- albinismo oculocutáneo pigmentario mínimo (trastorno)
- Minimal pigment oculocutaneous albinism (disorder)
- Platinum oculocutaneous albinism
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(61)Roll up to these when you need a wider cohort.
- 1Tyrosinase-negative oculocutaneous albinism
- 2Disorder of tyrosine metabolism
- 2Oculocutaneous albinism
- 3Albinism
- 3Autosomal recessive hereditary disorder
- 3Congenital oculocutaneous hypopigmentation
- 3Disorder of amino acid and organic acid metabolism
- 3Genetic disorder of skin pigmentation
- 3Hereditary disorder of the integument
- 3Hereditary disorder of the visual system
- 4Autosomal hereditary disorder
- 4Congenital anomaly of eye
- 4Congenital deficiency of pigment of skin
- 4Congenital malformation
- 4Developmental hereditary disorder
- 4Disorder of amino acid metabolism
- 4Disorder of integument
- 4Disorder of pigmentation
- 4Disorder of skin pigmentation
- 4Genetic disease
- 4Hereditary disorder by system
- 4Inborn error of metabolism
- 4Lesion of eye
- 4Visual system disorder
- 5Anomaly of eye
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