autosomal recessive nonsyndromic deafness 47

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Summary

Literature (0)

DOID:0110504 - autosomal recessive nonsyndromic deafness 47

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 2p25.1-p24.3.

Synonyms: autosomal recessive deafness 47, DFNB47

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:0012375 - autosomal recessive nonsyndromic hearing loss 47

MONDO:0012375 - autosomal recessive nonsyndromic hearing loss 47

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)