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Summary Literature (0)
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 : strc

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011364 - autosomal recessive nonsyndromic hearing loss 16

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive nonsyndromic deafness (is_a)