autosomal recessive nonsyndromic deafness 21

Summary

DOID:0110479 - autosomal recessive nonsyndromic deafness 21

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 TECTA gene on chromosome 11q23.3.

Synonyms: autosomal recessive deafness 21, DFNB21

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

: tecta.2, tecta

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011351 - autosomal recessive nonsyndromic hearing loss 21

MONDO:0011351 - autosomal recessive nonsyndromic hearing loss 21

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)