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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:0011994 - autosomal dominant nonsyndromic hearing loss 41 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee