autosomal recessive nonsyndromic deafness 40

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Summary

Literature (0)

DOID:0110499 - autosomal recessive nonsyndromic deafness 40

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 22q11.21-q12.1.

Synonyms: autosomal recessive deafness 40, DFNB40

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:0012002 - autosomal recessive nonsyndromic hearing loss 40

MONDO:0012002 - autosomal recessive nonsyndromic hearing loss 40

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)