autosomal recessive nonsyndromic deafness 2

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Summary

Literature (0)

DOID:0110477 - autosomal recessive nonsyndromic deafness 2

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.

Synonyms: autosomal recessive deafness 2, DFNB2

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

: myo7a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010807 - autosomal recessive nonsyndromic hearing loss 2

MONDO:0010807 - autosomal recessive nonsyndromic hearing loss 2

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)