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Summary Literature (0)
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: DFNB21, autosomal recessive deafness 21

Xenbase Genes : tecta.2, tecta.1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011351 - autosomal recessive nonsyndromic deafness 21

OMIM:
OMIM:603629 - DEAFNESS, AUTOSOMAL RECESSIVE 21; DFNB21

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive nonsyndromic deafness (is_a)