OMOP Concept 4189368
Congenital oculocutaneous hypopigmentation
StandardConditionSNOMED61649007Disorder
Maps from
1
Descendants
24
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 Congenital oculocutaneous hypopigmentation via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 61649007 | Congenital oculocutaneous hypopigmentation | Non-standard |
Synonyms
Alternative names recorded for Congenital oculocutaneous hypopigmentation across source vocabularies.
- Congenital oculocutaneous hypopigmentation (disorder)
- hipopigmentación oculocutánea congénita
- hipopigmentación oculocutánea congénita (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of eye
- 1Congenital deficiency of pigment of skin
- 1Lesion of eye
- 2Anomaly of eye
- 2Congenital anomaly of head
- 2Congenital anomaly of visual system
- 2Congenital pigmentary skin anomalies
- 2Skin hypopigmented
- 3Congenital anomaly of skin
- 3Congenital malformation
- 3Disorder of eye
- 3Disorder of head
- 3Disorder of skin pigmentation
- 3Visual system disorder
- 4Congenital anomaly of integument
- 4Congenital disease
- 4Developmental disorder
- 4Disease
- 4Disorder of body system
- 4Disorder of eye region
- 4Disorder of pigmentation
- 4Disorder of sensory organ
- 4Disorder of skin
- 4Eye / vision finding
- 4Globe finding
Narrower concepts
(24)Included automatically when you query with descendants.
- 1Oculocutaneous albinism
- 1Osteoporosis and oculocutaneous hypopigmentation syndrome
- 1Vici syndrome
- 1Waardenburg syndrome type 1
- 1Waardenburg syndrome type 2
- 2Black locks, oculocutaneous albinism, AND deafness of the sensorineural type
- 2COMMAD syndrome
- 2Cross syndrome
- 2Microcephalus with albinism and digital anomaly syndrome
- 2Oculocutaneous albinism type 1
- 2Oculocutaneous albinism type 4
- 2Oculocutaneous albinism type 5
- 2Oculocutaneous albinism type 6
- 2Oculocutaneous albinism type 7
- 2Oculocutaneous albinism type 8
- 2Tyrosinase-negative oculocutaneous albinism
- 2Tyrosinase-positive oculocutaneous albinism
- 3Brown oculocutaneous albinism
- 3Hermansky-Pudlak syndrome
- 3Minimal pigment oculocutaneous albinism
- 3Punctate oculocutaneous albinoidism
- 3Rufous albinism
- 3Temperature-sensitive oculocutaneous albinism
- 3Yellow mutant oculocutaneous albinism
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