autosomal dominant nonsyndromic deafness 21

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Summary

Literature (0)

DOID:0110551 - autosomal dominant nonsyndromic deafness 21

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 6p24.1-p22.3.

Synonyms: DFNA21, autosomal dominant deafness 21,

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

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Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011761 - autosomal dominant nonsyndromic hearing loss 21

MONDO:0011761 - autosomal dominant nonsyndromic hearing loss 21

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)