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DOID:0110483 - autosomal recessive nonsyndromic deafness 25
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the GRXCR1 gene on chromosome 4p13.
Synonyms: DFNB25, autosomal recessive deafness 25,
Echinobase Genes :
MIM:613285 - deafness, autosomal recessive 25; dfnb25 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee