OMOP Concept 4170892
Waardenburg syndrome
StandardConditionSNOMED47434006Disorder
Maps from
4
Descendants
5
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Waardenburg syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 122946 | Waardenburg's syndrome | Non-standard |
| MeSH | D014849 | Waardenburg Syndrome | Non-standard |
| Nebraska Lexicon | 47434006 | Waardenburg, types I AND/OR II | Non-standard |
| Read | PKy5400 | Waardenburg's syndrome | Non-standard |
Synonyms
Alternative names recorded for Waardenburg syndrome across source vocabularies.
- síndrome de Waardenburg
- síndrome de Waardenburg (trastorno)
- Waardenburg's syndrome
- Waardenburg syndrome (disorder)
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 deficiency of pigment of skin
- 1Congenital hearing disorder
- 1Decreased hearing
- 1Genetic disorder of skin pigmentation
- 1Hearing loss associated with syndrome
- 1Multiple system malformation syndrome
- 2Congenital disease
- 2Congenital malformation syndrome
- 2Congenital pigmentary skin anomalies
- 2Decline in functional status
- 2Disorder of skin pigmentation
- 2Genetic disease
- 2Hearing disorder
- 2Hearing finding
- 2Hearing loss
- 2Skin hypopigmented
- 3Congenital anomaly of skin
- 3Congenital malformation
- 3Disease
- 3Disorder of auditory system
- 3Disorder of fetus and/or newborn
- 3Disorder of pigmentation
- 3Ear and auditory finding
- 3Functional finding
- 3Skin lesion
Narrower concepts
(5)Included automatically when you query with descendants.
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