autosomal recessive nonsyndromic deafness 101

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Summary

Literature (0)

DOID:0110462 - autosomal recessive nonsyndromic deafness 101

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32.

Synonyms: autosomal recessive deafness 101, DFNB101

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

: grxcr2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014363 - autosomal recessive nonsyndromic hearing loss 101

MONDO:0014363 - autosomal recessive nonsyndromic hearing loss 101

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)