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Summary Literature (83)
DOID:0050736 - autosomal dominant disease


Disease Ontology Definition:An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease.

Synonyms:

Xenbase Genes : tbx1, c2, gdf2, wnt10a, slc24a4, tgfbr1, tnni2, dact1, fzd6, acvr1, mycn, avp, foxc1, fgfr3, eya1, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000426 - autosomal dominant disease


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal genetic disease (is_a)