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Summary Literature (0)
DOID:0110495 - autosomal recessive nonsyndromic deafness 37


Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.

Synonyms: DFNB37, autosomal recessive deafness 37

Xenbase Genes : myo6

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011912 - autosomal recessive nonsyndromic deafness 37

OMIM:
OMIM:607821 - DEAFNESS, AUTOSOMAL RECESSIVE 37; DFNB37

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)