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DOID:0110463 - autosomal recessive nonsyndromic deafness 102
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the EPS8 gene on chromosome 12p12.
Synonyms: DFNB102, autosomal recessive deafness 102,
Echinobase Genes :
MIM:615974 - deafness, autosomal recessive 102; dfnb102 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee