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Summary Literature (0)
DOID:0110574 - autosomal dominant nonsyndromic deafness 4B

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CEACAM16 gene on chromosome 19q13.

Synonyms: DFNA4B, autosomal dominant deafness 4B,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013823 - autosomal dominant nonsyndromic hearing loss 4B


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant nonsyndromic deafness (is_a)