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Summary Literature (0)
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.


Echinobase Genes : smad4, nf1, pitx2, ret, pax2, pkd2, eya1, tfap2a, flcn, nog, fgfr3, sufu, eftud2, pms1, mlh1, [+]

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)