Search Ontology:
Human Disease

Waardenburg syndrome type 2C

Term ID
DOID:0110951
Synonyms
  • Waardenburg syndrome type IIC
  • WS2C
Definition
A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in variation in the chromosome region 8p23. (2)
References
Ontology
Human Disease   ( DOID:0110951 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models