autosomal recessive nonsyndromic deafness 23

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Summary

Literature (0)

DOID:0110481 - autosomal recessive nonsyndromic deafness 23

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the PCDH15 gene on chromosome 10q21.

Synonyms: autosomal recessive deafness 23, DFNB23

Echinobase 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

: pcdh15

MIM:

MIM:609533 - deafness, autosomal recessive 23; dfnb23

MIM:609533 - deafness, autosomal recessive 23; dfnb23

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)