Search Ontology:
Human Disease
Waardenburg syndrome
- Term ID
- DOID:9258
- Synonyms
-
- van der Hoeve Halbertsona Waardenburg syndrome
- Waardenburg Shah syndrome
- Waardenburg's syndrome
- Waardenburg, types I and/or II
- Definition
- A syndrome characterized by varying degrees of deafness, minor defects in structures arising from the neural crest and pigmentation anomalies of the hair, the skin and/or the iris of both eyes. (3)
- References
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- GARD:5525
- MESH:D014849
- MIM:PS193500
- NCI:C75008
- NCI:C85222
- ORDO:3440
- ORDO:895
- SNOMEDCT_US_2023_03_01:1010606009
- SNOMEDCT_US_2023_03_01:190695000
- SNOMEDCT_US_2023_03_01:47434006
- UMLS_CUI:C0079661
- UMLS_CUI:C1847800
- UMLS_CUI:C3266898
- Ontology
- Human Disease ( DOID:9258 )
- is a type of
-
- has subtype
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Genes Involved
Zebrafish Models