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DOID:0111738 - X-linked deafness 7
Disease Ontology Definition:An X-linked nonsyndromic deafness characterized by congenital, bilateral, mixed or conductive hearing loss and other ear anomalies that has_material_basis_in homozygous or hemizygous mutation in the GPRASP2 gene on chromosome Xq22.1.
Synonyms: DFNX7, X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome,
Xenbase Genes :
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)