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Human Disease

Waardenburg syndrome type 2B

Term ID
DOID:0110947
Synonyms
  • Waardenburg syndrome type IIB
  • WS2B
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 1p21-p13.3. (2)
References
Ontology
Human Disease   ( DOID:0110947 )
Relationships
is a type of
disjoint_from
Other Pages
Genes Involved
Zebrafish Models