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DOID:2236 - congenital afibrinogenemia
Disease Ontology Definition:n_a
Synonyms: Factor I deficiency, Fibrinogen deficiency,
Echinobase Genes :
MIM:202400 - afibrinogenemia, congenital hypofibrinogenemia, congenital, included |
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)