MeSH Browser

MeSH Heading: Protein C Deficiency
Tree Number(s): C15.378.100.100.690; C15.378.147.880; C15.378.925.795; C16.320.099.690
Unique ID: D020151
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D020151
Scope Note: An absence or deficiency in PROTEIN C which leads to impaired regulation of blood coagulation. It is associated with an increased risk of severe or premature thrombosis. (Stedman's Med. Dict., 26th ed.)
Entry Version: PROTEIN C DEFIC
Entry Term(s): Deficiency, Protein C; Hereditary Thrombophilia Due To Protein C Deficiency
Previous Indexing: Blood Proteins (1981-1987); Glycoproteins (1981-1987); Protein C (1987-1998)
See Also: Activated Protein C Resistance
Public MeSH Note: 99
History Note: 99
Date Established: 1999/01/01
Date of Entry: 1998/06/10
Revision Date: 2013/07/08

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)

Protein C Deficiency MeSH Descriptor Data 2024