autosomal recessive nonsyndromic deafness 16

Summary

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: autosomal recessive deafness 16, DFNB16

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: strc

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011364 - cleidocephalicus muscle

MONDO:0011364 - cleidocephalicus muscle

MIM:

MIM:603720 - DEAFNESS, AUTOSOMAL RECESSIVE 16; DFNB16

MIM:603720 - DEAFNESS, AUTOSOMAL RECESSIVE 16; DFNB16

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive nonsyndromic deafness (is_a)