autosomal recessive nonsyndromic deafness 76

Summary

DOID:0110524 - autosomal recessive nonsyndromic deafness 76

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with high frequency, progressive hearing loss and has_material_basis_in mutation in the SYNE4 gene on chromosome 19q13.

Synonyms: DFNB76, autosomal recessive deafness 76,

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

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Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014237 - autosomal recessive nonsyndromic hearing loss 76

MONDO:0014237 - autosomal recessive nonsyndromic hearing loss 76

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)