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Summary Literature (0)
DOID:0080261 - autosomal recessive nonsyndromic deafness 106


Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous mutation in the EPS8L2 gene on chromosome 11p15.

Synonyms:

Xenbase Genes : eps8l2



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)