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Summary Literature (0)
DOID:0110567 - autosomal dominant nonsyndromic deafness 41


Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has_material_basis_in mutation in the P2RX2 gene on chromosome 12q24.

Synonyms: DFNA41, autosomal dominant deafness 41

Xenbase Genes : p2rx2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011994 - autosomal dominant nonsyndromic deafness 41

OMIM:
OMIM:608224 - DEAFNESS, AUTOSOMAL DOMINANT 41; DFNA41

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)