autosomal recessive nonsyndromic deafness 18A

Summary

DOID:0110473 - autosomal recessive nonsyndromic deafness 18A

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 USH1C gene on chromosome 11p15.

Synonyms: autosomal recessive deafness 18A, DFNB18A

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

: ush1c

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011192 - autosomal recessive nonsyndromic hearing loss 18A

MONDO:0011192 - autosomal recessive nonsyndromic hearing loss 18A

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)