NLM Logo

Afibrinogenemia MeSH Descriptor Data 2022


MeSH Heading
Afibrinogenemia
Tree Number(s)
C15.378.100.100.056
C15.378.100.141.072
C15.378.463.067
C16.320.099.056
Unique ID
D000347
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000347
Scope Note
A deficiency or absence of FIBRINOGEN in the blood.
Entry Term(s)
Afibrinogenemia, Congenital
Congenital Afibrinogenaemia
Congenital Afibrinogenemia
Deficiency, Fibrinogen
Familial Afibrinogenemia
Fibrinogen Deficiency
Hypofibrinogenemia, Congenital
NLM Classification #
WH 322
Date Established
1966/01/01
Date of Entry
1999/01/01
Revision Date
2018/06/13
Afibrinogenemia Preferred
Congenital Afibrinogenemia Related
Deficiency, Fibrinogen Narrower
page delivered in 0.181s