Structured Summary
Abstract
A deficiency or absence of FIBRINOGEN in the blood.
MeSH Record
Classification
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MeSH Record
Synonyms
20 entry terms
- Afibrinogenemias
- Afibrinogenemia, Congenital
- Congenital Afibrinogenaemia
- Congenital Afibrinogenemia
- Deficiency, Fibrinogen
- Familial Afibrinogenemia
- Fibrinogen Deficiency
- Hypofibrinogenemia, Congenital
- Afibrinogenaemia, Congenital
- Afibrinogenaemias, Congenital
- Afibrinogenemia, Familial
- Afibrinogenemias, Congenital
- Afibrinogenemias, Familial
- Congenital Afibrinogenaemias
- Congenital Afibrinogenemias
- Congenital Hypofibrinogenemia
- Congenital Hypofibrinogenemias
- Familial Afibrinogenemias
- Fibrinogen Deficiencies
- Hypofibrinogenemias, Congenital
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Hierarchy
Tree Numbers
MeSH Record
NLM Classification
WH 322
AMA Style
References
- National Library of Medicine. Afibrinogenemia. Medical Subject Headings (MeSH). 2026. Unique ID D000347. http://id.nlm.nih.gov/mesh/2026/D000347
- Afibrinogenemia. In: Wikipedia. https://en.wikipedia.org/wiki/Congenital_afibrinogenemia
- Afibrinogenemia. In: Wikidata. https://www.wikidata.org/wiki/Q5160407