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: DFNB2, autosomal recessive deafness 2,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: myo7a

OMIM:

MIM:600060 - deafness, autosomal recessive 2; dfnb2

MIM:600060 - deafness, autosomal recessive 2; dfnb2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive nonsyndromic deafness (is_a)