autosomal recessive nonsyndromic deafness 91

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Summary

Literature (0)

DOID:0110536 - autosomal recessive nonsyndromic deafness 91

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the SERPINB6 gene on chromosome 6p25.

Synonyms: DFNB91, autosomal recessive deafness 91,

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

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

: serpinb6

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013269 - autosomal recessive nonsyndromic hearing loss 91

MONDO:0013269 - autosomal recessive nonsyndromic hearing loss 91

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)