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Summary Literature (0)
DOID:0110489 - autosomal recessive nonsyndromic deafness 30


Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutations in the MYO3A gene on chromosome 10p12.1.

Synonyms: DFNB30, autosomal recessive deafness 30

In OMIM:
OMIM:607101 - DEAFNESS, AUTOSOMAL RECESSIVE 30; DFNB30

In Mondo Disease Ontology:
MONDO:0011774 - autosomal recessive nonsyndromic deafness 30

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : myo3a

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal recessive nonsyndromic deafness (is_a)