autosomal recessive nonsyndromic deafness 62

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Summary

Literature (0)

DOID:0110514 - autosomal recessive nonsyndromic deafness 62

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 12p13.2-p11.23.

Synonyms: DFNB62, autosomal recessive deafness 62,

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:0012418 - autosomal recessive nonsyndromic hearing loss 62

MONDO:0012418 - autosomal recessive nonsyndromic hearing loss 62

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)