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Summary Literature (0)
DOID:0110569 - autosomal dominant nonsyndromic deafness 44


Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized postlingual onset with low to mild frequency progressive hearing loss and has_material_basis_in mutation in the CCDC50 gene on chromosome 3q28.

Synonyms: DFNA44, autosomal dominant deafness 44

In OMIM:
OMIM:607453 - DEAFNESS, AUTOSOMAL DOMINANT 44; DFNA44

In Mondo Disease Ontology:
MONDO:0011832 - autosomal dominant nonsyndromic deafness 44

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : ccdc50

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant nonsyndromic deafness (is_a)