MeSH Browser

MeSH Heading: Factor X Deficiency
Tree Number(s): C15.378.100.100.320; C15.378.100.141.320; C15.378.463.320; C16.320.099.320
Unique ID: D005171
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D005171
Annotation: a blood coag disord
Scope Note: Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
Entry Version: FACTOR X DEFIC
Entry Term(s): Deficiency, Factor 10; Deficiency, Factor Ten; Deficiency, Factor X; Deficiency, Stuart-Prower; Deficiency, Stuart-Prower Factor; Factor 10 Deficiency; Factor Ten Deficiency; Stuart-Prower Deficiency; Stuart-Prower Factor Deficiency
Public MeSH Note: 91; was see under HYPOPROTHROMBINEMIAS 1975-90
Online Note: search HYPOPROTHROMBINEMIAS 1966-74
History Note: 91(75); was see under HYPOPROTHROMBINEMIAS 1975-90
Date Established: 1991/01/01
Date of Entry: 1999/01/01
Revision Date: 2017/05/02

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)

Concept UI: M0008155
Scope Note: Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
Terms: Factor X Deficiency Preferred Term
Term UI T015828
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1975); Deficiency, Factor Ten
Term UI T000913554
Date01/04/2017
LexicalTag NON
ThesaurusID NLM (2018); Factor 10 Deficiency
Term UI T000913555
Date01/04/2017
LexicalTag NON
ThesaurusID NLM (2018); Factor Ten Deficiency
Term UI T000913556
Date01/04/2017
LexicalTag NON
ThesaurusID NLM (2018); Stuart-Prower Factor Deficiency
Term UI T015832
Date04/24/1989
LexicalTag EPO
ThesaurusID NLM (1990); Deficiency, Stuart-Prower
Term UI T015829
Date06/17/1991
LexicalTag EPO
ThesaurusID NLM (1992); Stuart-Prower Deficiency
Term UI T015830
Date04/24/1989
LexicalTag EPO
ThesaurusID NLM (1990); Deficiency, Stuart-Prower Factor
Term UI T015831
Date06/17/1991
LexicalTag EPO
ThesaurusID NLM (1992); Deficiency, Factor 10
Term UI T000913553
Date01/04/2017
LexicalTag NON
ThesaurusID NLM (2018); Deficiency, Factor X
Term UI T015827
Date01/01/1986
LexicalTag NON
ThesaurusID UNK (19XX)

Factor X Deficiency MeSH Descriptor Data 2024