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DOID:0110500 - autosomal recessive nonsyndromic deafness 42
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the ILDR1 gene on chromosome 3q13.
Synonyms: autosomal recessive deafness 42, DFNB42
Xenbase Genes : ildr1
MONDO:0012326 - autosomal recessive nonsyndromic hearing loss 42 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee