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DOID:0110494 - autosomal recessive nonsyndromic deafness 36
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36.
Synonyms: DFNB36, autosomal recessive deafness 36,
Xenbase Genes : espn
MONDO:0012170 - autosomal recessive nonsyndromic hearing loss 36 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee