congenital afibrinogenemia
Human disease
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congenital afibrinogenemia
Summary
congenital afibrinogenemia is a class of disease[1].
Key Facts
- congenital afibrinogenemia's instance of is recorded as class of disease[2].
- congenital afibrinogenemia is a type of Factor I Deficiency[3].
- congenital afibrinogenemia is a type of inherited blood coagulation disease[4].
- congenital afibrinogenemia is a type of autosomal recessive disease[5].
- congenital afibrinogenemia is a type of blood coagulation disease[6].
- congenital afibrinogenemia's NCI Thesaurus ID is recorded as C98130[7].
- congenital afibrinogenemia's health specialty is recorded as hematology[8].
- congenital afibrinogenemia's genetic association is recorded as FGG[9].
- congenital afibrinogenemia's genetic association is recorded as FGB[10].
- congenital afibrinogenemia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2236[11].
- congenital afibrinogenemia's exact match is recorded as http://identifiers.org/doid/DOID:2236[12].
- congenital afibrinogenemia's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].