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Summary Literature (0)
DOID:0110484 - autosomal recessive nonsyndromic deafness 26


Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 4q31.

Synonyms: autosomal recessive deafness 26, DFNB26

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011553 - autosomal recessive nonsyndromic hearing loss 26


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)