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DOID:0111735 - X-linked deafness 4
Disease Ontology Definition:An X-linked nonsyndromic deafness characterized by progressive hearing loss with postlingual onset and earlier onset in males compared to females that has_material_basis_in mutation in the SMPX gene on chromosome Xp22.12.
Synonyms: DFN6, DFNX4, nonsyndromic sensorineural progressive deafness 6, X-linked progressive deafness 6
Xenbase Genes

MIM:300066 - DEAFNESS, X-LINKED 4; DFNX4 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
X-linked nonsyndromic deafness (is_a)