"Afibrinogenemia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A deficiency or absence of FIBRINOGEN in the blood.
Descriptor ID |
D000347
|
MeSH Number(s) |
C15.378.100.100.056 C15.378.100.141.072 C15.378.463.067 C16.320.099.056
|
Concept/Terms |
Afibrinogenemia- Afibrinogenemia
- Afibrinogenemias
- Fibrinogen Deficiency
- Deficiency, Fibrinogen
- Fibrinogen Deficiencies
Congenital Afibrinogenemia- Congenital Afibrinogenemia
- Afibrinogenemia, Congenital
- Afibrinogenemias, Congenital
- Congenital Afibrinogenemias
- Familial Afibrinogenemia
- Afibrinogenemia, Familial
- Afibrinogenemias, Familial
- Familial Afibrinogenemias
- Congenital Afibrinogenaemia
- Afibrinogenaemia, Congenital
- Afibrinogenaemias, Congenital
- Congenital Afibrinogenaemias
- Hypofibrinogenemia, Congenital
- Congenital Hypofibrinogenemia
- Congenital Hypofibrinogenemias
- Hypofibrinogenemias, Congenital
|
Below are MeSH descriptors whose meaning is more general than "Afibrinogenemia".
Below are MeSH descriptors whose meaning is more specific than "Afibrinogenemia".
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Below are the most recent publications written about "Afibrinogenemia" by people in Profiles.