OBO ID: DOID:0110947
Term Name: Waardenburg syndrome type 2B Search Ontology:
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 Waardenburg syndrome type 2B PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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