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Summary Literature (60)
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:

Referenced OMIM:

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : tbx1, c2, gdf2, wnt10a, tnni2, acvr1, mycn, foxc1, fgfr3, eya1, sufu, cfb, hras, ttr, zeb2, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal genetic disease (is_a)


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