autosomal dominant nonsyndromic deafness 40

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Summary

Literature (0)

DOID:0110566 - autosomal dominant nonsyndromic deafness 40

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CRYM gene on chromosome 16p12.

Synonyms: autosomal dominant deafness 40, DFNA40

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

: crym

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014603 - autosomal dominant nonsyndromic hearing loss 40

MONDO:0014603 - autosomal dominant nonsyndromic hearing loss 40

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant nonsyndromic deafness (is_a)