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Summary Literature (0)
DOID:2216 - factor V deficiency

Disease Ontology Definition:n_a

Synonyms: deficiency, labile, Hereditary hypoproaccelerinaemia, Labile factor deficiency, Proaccelerin deficiency

Xenbase Genes : f5

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009210 - pharyngeal membrane

MIM:
MIM:227400 - FACTOR V DEFICIENCY

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

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