factor x deficiency

Preferred Label : factor x deficiency;

MeSH definition : 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.;

MeSH synonym : deficiency, stuart-prower; deficiency, stuart prower factor; stuart-prower deficiency; deficiencies, factor x; stuart-prower factor deficiency; stuart prower deficiency; deficiency, stuart-prower factor; deficiency, factor x; factor x deficiencies; deficiency, stuart prower; stuart prower factor deficiency; Deficiency, Factor Ten; Deficiencies, Factor Ten; Factor Ten Deficiencies; Ten Deficiencies, Factor; Factor 10 Deficiency; Factor Ten Deficiency; Deficiency, Factor 10; Deficiencies, Factor 10; Factor 10 Deficiencies;

MeSH annotation : a blood coag disord; DF: FACTOR X DEFIC; a blood coag disord;

Wikipedia link : https://en.wikipedia.org/wiki/Factor x deficiency;

Details

Origin ID

D005171;

UMLS CUI

C0015519;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Complement factor D deficiency [OMIM Phenotype]
- Complement factor h deficiency [OMIM Phenotype]
- Factor II deficiency [MedDRA Preferred Term]
- Factor III deficiency [MedDRA Preferred Term]
- Factor V deficiency [OMIM Phenotype]
- Factor V deficiency [MedDRA Preferred Term]
- Hereditary Factor X Deficiency [NCIt concept]
- Hereditary factor X deficiency [ICD-11 Subcategory]
- Hereditary factor X deficiency disease (disorder) [SNOMED CT concept]
- PROTHROMBIN TIME PROLONGED [WHO-ART Included Term]
- factor X deficiency [DO Concept]
- factor ii deficiency [TUV Concept]
- factor ii deficiency, nos [SNOMED Notion]
- factor v deficiency, nos [SNOMED Notion]
- hereditary factor x deficiency disease [SNOMED Notion]
Currated CISMeF NLP mapping
- Congenital factor X deficiency [ORDO Disease]
- Factor X Deficiency [NCIt concept]
- Factor X deficiency [PASCAL descriptor]
- Factor X deficiency [MedDRA Preferred Term]
- Factor X deficiency [OMIM Phenotype]
- Factor X deficiency (disorder) [SNOMED CT concept]
- Reduced factor X activity [HPO term]
- blood clotting factor x deficiency [Disease (Nov.)]
- factor x deficiency [Blood Transfusion thesaurus concept]
- factor x deficiency, nos [SNOMED Notion]
DO Cross reference
- factor X deficiency [DO Concept]
HPO term
- Reduced factor X activity [HPO term]
Has phenotype(s) (HPO)
- Hemarthroses [HPO term]
Manual NTBT mappings (CISMeF)
- Congenital vitamin K-dependent coagulation factors deficiency [ORDO Disease]
MeSH Descriptor(s) used for indexing
- factor X [MeSH Descriptor]
- factor xa [MeSH Descriptor]
Record concept(s)
- factor X deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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