OMOP Concept 4029099
Waardenburg syndrome type 3
StandardConditionSNOMED237918004Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Waardenburg syndrome type 3 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 136255 | Klein-Waardenberg's Syndrome | Non-standard |
| Nebraska Lexicon | 237918004 | Klein-Waardenberg syndrome | Non-standard |
| Read | C302711 | Klein-Waardenberg's syndrome | Non-standard |
Synonyms
Alternative names recorded for Waardenburg syndrome type 3 across source vocabularies.
- Klein-Waardenberg's syndrome
- Klein-Waardenberg syndrome
- síndrome de Klein-Waardenberg
- síndrome de Waardenburg tipo 3
- síndrome de Waardenburg tipo 3 (trastorno)
- síndrome de Waardenburg tipo III
- Waardenburg syndrome type 3 (disorder)
- Waardenburg syndrome type III
- Waardenburg syndrome with limb anomalies
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(67)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of limb
- 1Congenital sensorineural hearing loss
- 1Dystopia canthorum
- 1Multiple malformation syndrome with limb defect as major feature
- 1Waardenburg syndrome
- 2Congenital deficiency of pigment of skin
- 2Congenital hearing disorder
- 2Congenital malformation
- 2Congenital structural abnormality of eyelid
- 2Decreased hearing
- 2Disorder of limb
- 2Genetic disorder of skin pigmentation
- 2Hearing loss associated with syndrome
- 2Medial canthus finding
- 2Multiple system malformation syndrome
- 2Sensorineural hearing loss
- 3Congenital anomaly of face
- 3Congenital anomaly of ocular adnexa
- 3Congenital disease
- 3Congenital malformation syndrome
- 3Congenital pigmentary skin anomalies
- 3Decline in functional status
- 3Developmental disorder
- 3Disease
- 3Disorder of eyelid
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