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Summary Literature (0)
DOID:0110563 - autosomal dominant nonsyndromic deafness 36


Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the TMC1 gene on chromosome 9q21.

Synonyms: DFNA36, autosomal dominant deafness 36

Xenbase Genes : tmc1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011708 - autosomal dominant nonsyndromic hearing loss 36

OMIM:
OMIM:606705 - DEAFNESS, AUTOSOMAL DOMINANT 36; DFNA36

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

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