autosomal recessive nonsyndromic deafness 63

Summary

DOID:0110515 - autosomal recessive nonsyndromic deafness 63

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 LRTOMT gene on chromosome 11q13.

Synonyms: autosomal recessive deafness 63, DFNB63

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

: lrtomt

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012670 - autosomal recessive nonsyndromic hearing loss 63

MONDO:0012670 - autosomal recessive nonsyndromic hearing loss 63

MIM:

MIM:611451 - DEAFNESS, AUTOSOMAL RECESSIVE 63; DFNB63

MIM:611451 - DEAFNESS, AUTOSOMAL RECESSIVE 63; DFNB63

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)