autosomal recessive nonsyndromic deafness 66

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Summary

Literature (0)

DOID:0110517 - autosomal recessive nonsyndromic deafness 66

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the DCDC2 gene on chromosome 6p22.

Synonyms: DFNB66, autosomal recessive deafness 66,

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:0012442 - autosomal recessive nonsyndromic hearing loss 66

MONDO:0012442 - autosomal recessive nonsyndromic hearing loss 66

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)