autosomal recessive nonsyndromic deafness 42

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Summary

Literature (0)

DOID:0110500 - autosomal recessive nonsyndromic deafness 42

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the ILDR1 gene on chromosome 3q13.

Synonyms: DFNB42, autosomal recessive deafness 42,

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

: ildr1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012326 - autosomal recessive nonsyndromic hearing loss 42

MONDO:0012326 - autosomal recessive nonsyndromic hearing loss 42

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)