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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: DFNB29, autosomal recessive deafness 29,
Xenbase Genes : cldn14
MONDO:0013537 - autosomal recessive nonsyndromic hearing loss 29 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee