autosomal recessive nonsyndromic deafness 86

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Summary

Literature (0)

DOID:0110532 - autosomal recessive nonsyndromic deafness 86

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13.

Synonyms: autosomal recessive deafness 86, DFNB86

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

: tbc1d24

OMIM:

MIM:614617 - deafness, autosomal recessive 86; dfnb86

MIM:614617 - deafness, autosomal recessive 86; dfnb86

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)