autosomal recessive nonsyndromic deafness 88

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Summary

Literature (0)

DOID:0110533 - autosomal recessive nonsyndromic deafness 88

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the ELMOD3 gene on chromosome 2p11.

Synonyms: autosomal recessive deafness 88, DFNB88

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

: elmod3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014182 - autosomal recessive nonsyndromic hearing loss 88

MONDO:0014182 - autosomal recessive nonsyndromic hearing loss 88

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)