autosomal recessive nonsyndromic deafness 29

Summary

DOID:0110487 - autosomal recessive nonsyndromic deafness 29

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 CLDN14 gene on chromosome 21q22.

Synonyms: autosomal recessive deafness 29, DFNB29

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

: cldn14

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013537 - autosomal recessive nonsyndromic hearing loss 29

MONDO:0013537 - autosomal recessive nonsyndromic hearing loss 29

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)