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DOID:2235 - prothrombin deficiency
Disease Ontology Definition:n_a
Synonyms: Factor II deficiency, hypoprothrombinemia,
Echinobase Genes :
MIM:613679 - prothrombin deficiency, congenital |
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)