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DOID:0110505 - autosomal recessive nonsyndromic deafness 48
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the CIB2 gene on chromosome 15q25.
Synonyms: autosomal recessive deafness 48, DFNB48
Xenbase Genes : cib2
MONDO:0012273 - autosomal recessive nonsyndromic hearing loss 48 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee