OMOP Concept 605211
Waardenburg syndrome type 2
StandardConditionSNOMED1010636000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2021
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Waardenburg syndrome type 2 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536463 | Waardenburg syndrome type 2 | Non-standard |
Synonyms
Alternative names recorded for Waardenburg syndrome type 2 across source vocabularies.
- síndrome de Waardenburg tipo 2
- síndrome de Waardenburg tipo 2 (trastorno)
- síndrome de Waardenburg tipo II
- Waardenburg syndrome type 2 (disorder)
- Waardenburg syndrome type II
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(62)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of hair
- 1Congenital oculocutaneous hypopigmentation
- 1Waardenburg syndrome
- 2Congenital anomaly of eye
- 2Congenital anomaly of skin
- 2Congenital deficiency of pigment of skin
- 2Congenital hearing disorder
- 2Decreased hearing
- 2Disorder of hair
- 2Genetic disorder of skin pigmentation
- 2Hearing loss associated with syndrome
- 2Lesion of eye
- 2Multiple system malformation syndrome
- 2Structural abnormality of skin appendage
- 3Anomaly of eye
- 3Congenital anomaly of head
- 3Congenital anomaly of integument
- 3Congenital anomaly of visual system
- 3Congenital disease
- 3Congenital malformation syndrome
- 3Congenital pigmentary skin anomalies
- 3Decline in functional status
- 3Disorder of skin
- 3Disorder of skin appendage
- 3Disorder of skin pigmentation
Showing 25 of 62. Retrieve the full set via the API.
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