OMOP Concept 37396221
Waardenburg Shah syndrome
StandardConditionSNOMED715952000Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Waardenburg Shah syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536467 | Waardenburg syndrome, type 4 | Non-standard |
| Nebraska Lexicon | 715952000 | Waardenburg syndrome co-occurrent with Hirschsprung disease | Non-standard |
Synonyms
Alternative names recorded for Waardenburg Shah syndrome across source vocabularies.
- Shah Waardenburg syndrome
- síndrome de Waardenburg concomitante con enfermedad de Hirschsprung
- síndrome de Waardenburg Shah
- síndrome de Waardenburg Shah (trastorno)
- Waardenburg Hirschsprung syndrome
- Waardenburg Shah syndrome (disorder)
- Waardenburg syndrome co-occurrent with Hirschsprung disease
- Waardenburg syndrome type 4
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(103)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Autosomal hereditary disorder
- 1Congenital aganglionic megacolon
- 1Congenital sensorineural hearing loss
- 1Developmental hereditary disorder
- 1Digestive system hereditary disorder
- 1Hereditary disorder of the integument
- 1Inherited autonomic nervous system disorder
- 1Waardenburg syndrome
- 2Aganglionosis of large intestine
- 2Congenital anomaly of the peripheral nervous system
- 2Congenital deficiency of pigment of skin
- 2Congenital dilatation of intestinal tract
- 2Congenital hearing disorder
- 2Decreased hearing
- 2Developmental disorder
- 2Dilatation of large intestine
- 2Disorder of auditory system
- 2Disorder of autonomic nervous system
- 2Disorder of digestive system
- 2Disorder of integument
- 2Genetic disorder of skin pigmentation
- 2Hearing loss associated with syndrome
- 2Hereditary disease
- 2Hereditary disorder by system
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