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DOID:2216 - factor V deficiency
Disease Ontology Definition:n_a
Synonyms: Hereditary hypoproaccelerinaemia, Labile factor deficiency, Proaccelerin deficiency, deficiency, labile,
Xenbase Genes : f5
MONDO:0009210 - congenital factor V deficiency |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee