Congenital hypofibrinogenemia

CaLiGraph

Property	Value
rdf:type	Coagulopathie owl:NamedIndividual Fibrinogen disorder Autosomal recessive disorder Congenital disorder Disease of liver
rdfs:label	Congenital hypofibrinogenemia
owl:sameAs	dbr:Congenital_hypofibrinogenemia
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Congenital_disorders http://en.wikipedia.org/wiki/Category:Coagulopathies http://en.wikipedia.org/wiki/Placental_abruption http://en.wikipedia.org/wiki/List_of_diseases_(H) http://en.wikipedia.org/wiki/Cryoprecipitate http://en.wikipedia.org/wiki/Factor_I_deficiency http://en.wikipedia.org/wiki/List_of_fibrinogen_disorders http://en.wikipedia.org/wiki/Category:Diseases_of_liver http://en.wikipedia.org/wiki/List_of_congenital_disorders http://en.wikipedia.org/wiki/Category:Autosomal_recessive_disorders
skos:prefLabel	Congenital hypofibrinogenemia
skos:altLabel	Fibrinogen storage disease Hypofibrinogenemia, familial
clgo:eMedicineSubject	article
clgo:eMedicineTopic	960677

About: clgr:Congenital_hypofibrinogenemia