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DOID:0110471 - autosomal recessive nonsyndromic deafness 16
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the STRC gene on chromosome 15q15.
Synonyms: DFNB16, autosomal recessive deafness 16
Xenbase Genes

MONDO:0011364 - autosomal recessive nonsyndromic hearing loss 16 |
OMIM:603720 - DEAFNESS, AUTOSOMAL RECESSIVE 16; DFNB16 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee