autosomal recessive nonsyndromic deafness 77

Summary

DOID:0110525 - autosomal recessive nonsyndromic deafness 77

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the LOXHD1 gene on chromosome 18q21.

Synonyms: DFNB77, autosomal recessive deafness 77,

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

: loxhd1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013119 - autosomal recessive nonsyndromic hearing loss 77

MONDO:0013119 - autosomal recessive nonsyndromic hearing loss 77

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)