MeSH Browser

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

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Afibrinogenemia MeSH Descriptor Data 2024