autosomal recessive nonsyndromic deafness 25

Summary

DOID:0110483 - autosomal recessive nonsyndromic deafness 25

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the GRXCR1 gene on chromosome 4p13.

Synonyms: autosomal recessive deafness 25, DFNB25

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

: grxcr1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013210 - autosomal recessive nonsyndromic hearing loss 25

MONDO:0013210 - autosomal recessive nonsyndromic hearing loss 25

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)