MeSH Browser

MeSH Heading: Blood Coagulation Disorders, Inherited
Tree Number(s): C15.378.100.100; C16.320.099
Unique ID: D025861
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D025861
Scope Note: Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.
Entry Version: BLOOD COAG DIS INHERITED
Entry Term(s): Coagulation Disorders, Inherited; Hereditary Blood Coagulation Disorders; Hereditary Coagulation Disorders; Inherited Blood Coagulation Disorders; Inherited Coagulation Disorders
NLM Classification #: WH 322
Previous Indexing: Blood Coagulation Disorders (1995-2001)
Public MeSH Note: 2002
History Note: 2002
Date Established: 2002/01/01
Date of Entry: 2001/07/25
Revision Date: 2006/07/05

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

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)

Blood Coagulation Disorders, Inherited MeSH Descriptor Data 2024