Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0050177 - monogenic disease


Disease Ontology Definition:A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.

Synonyms:

Xenbase Genes : foxh1.2, tbx1, hba1, gdf9, c2, gata2, gdf2, fzd4, suclg1, wnt10a, tcf3, slc24a4, rab28, fgg, pygl, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000275 - obsolete monogenic disease


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

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