autosomal recessive nonsyndromic deafness 98

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Summary

Literature (0)

DOID:0110540 - autosomal recessive nonsyndromic deafness 98

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TSPEAR gene on chromosome 21q22.

Synonyms: autosomal recessive deafness 98, DFNB98

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

: tspear

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013929 - autosomal recessive nonsyndromic hearing loss 98

MONDO:0013929 - autosomal recessive nonsyndromic hearing loss 98

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)