NIH MeSH · D000347Diseases
Afibrinogenemia
Also known asAfibrinogenemias · Congenital Afibrinogenemia · Congenital Afibrinogenaemia · Afibrinogenaemia, Congenital · Afibrinogenaemias, Congenital · Congenital Afibrinogenaemias · Afibrinogenemia, Congenital · Afibrinogenemias, Congenital · Congenital Afibrinogenemias · Hypofibrinogenemia, Congenital · Congenital Hypofibrinogenemia · Congenital Hypofibrinogenemias
Definition
A deficiency or absence of FIBRINOGEN in the blood.
MeSH classification
- C15.378.100.100.056
- C15.378.100.141.072
- C15.378.463.067
- C16.320.099.056
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Common questions about Afibrinogenemia
What does Afibrinogenemia mean in medicine?
A deficiency or absence of FIBRINOGEN in the blood. This definition is taken from the National Library of Medicine's MeSH (Medical Subject Headings) 2026 release, which is the standard vocabulary used to index PubMed and most medical literature.
Is Afibrinogenemia known by any other names?
Yes. Afibrinogenemia is also referred to as Afibrinogenemias, Congenital Afibrinogenemia, Congenital Afibrinogenaemia, Afibrinogenaemia, Congenital in different clinical, research and patient-facing contexts. The MeSH descriptor groups all of these synonyms under a single canonical concept so research and records stay consistent.
Where does Afibrinogenemia sit in the medical classification?
Afibrinogenemia falls under the broader medical category "Diseases" in the MeSH hierarchy (tree numbers: C15.378.100.100.056, C15.378.100.141.072, C15.378.463.067). Browsing the related concepts on this page takes you to neighbouring topics in the same branch of medicine.
Where can I get a plain-language explanation of Afibrinogenemia?
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Source: NIH MeSH 2026 (D000347) — National Library of Medicine, public domain. View official MeSH record ↗