factor V deficiency

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Summary

Literature (0)

DOID:2216 - factor V deficiency

Disease Ontology Definition:n_a

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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: f5

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009210 - congenital factor V deficiency

MONDO:0009210 - congenital factor V deficiency

Other Model Organisms: AGR, 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)