autosomal recessive nonsyndromic deafness 20

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Summary

Literature (0)

DOID:0110478 - autosomal recessive nonsyndromic deafness 20

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 11q25-qter.

Synonyms: DFNB20, autosomal recessive deafness 20,

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:0011392 - autosomal recessive nonsyndromic hearing loss 20

MONDO:0011392 - autosomal recessive nonsyndromic hearing loss 20

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)