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DOID:2216 - factor V deficiency
Disease Ontology Definition:n_a
Synonyms: Hereditary hypoproaccelerinaemia, Labile factor deficiency, Proaccelerin deficiency, deficiency, labile,
Echinobase Genes :
MIM:227400 - factor v deficiency |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
inherited blood coagulation disease (is_a)