hypoprothrombinemias

Preferred Label : hypoprothrombinemias;

MeSH definition : Absence or reduced levels of PROTHROMBIN in the blood.;

MeSH synonym : deficiencies, factor ii; prothrombin deficiencies; factor ii deficiencies; deficiency, factor ii; hypoprothrombinemia; deficiency, prothrombin; prothrombin deficiency; deficiencies, prothrombin; factor ii deficiency;

Wikipedia link : https://en.wikipedia.org/wiki/Hypoprothrombinemias;

Détails

Origin ID

D007020;

UMLS CUI

C4722227;

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 [NCIt concept]
- Factor III deficiency [MedDRA Preferred Term]
- Factor V deficiency [OMIM Phenotype]
- Factor V deficiency [MedDRA Preferred Term]
- Factor X deficiency [PASCAL descriptor]
- Factor X deficiency [OMIM Phenotype]
- Factor X deficiency [MedDRA Preferred Term]
- Hereditary factor II deficiency [ICD-11 More detail]
- Hypoprothrombinemia [PASCAL descriptor]
- Prothrombin deficiency, congenital [OMIM Phenotype]
- factor II deficiency [Blood Transfusion thesaurus concept]
- factor v deficiency, nos [SNOMED Notion]
- factor x deficiency, nos [SNOMED Notion]
- prothrombin deficiency [DO Concept]
Currated CISMeF NLP mapping
- Factor II deficiency [MedDRA Preferred Term]
- Factor II deficiency (disorder) [SNOMED CT concept]
- HYPOPROTHROMBINAEMIA [WHO-ART Included Term]
- Hereditary Factor II Deficiency [NCIt concept]
- Hypoprothrombinaemia [ICD-11 More detail]
- Hypoprothrombinaemia [MedDRA Preferred Term]
- Hypoprothrombinemia [MedDRA LLT]
- PROTHROMBIN TIME PROLONGED [WHO-ART Included Term]
- Prothrombin deficiency [MedDRA LLT]
- factor ii deficiency [TUV Concept]
- factor ii deficiency, nos [SNOMED Notion]
Indexing information
- prothrombin habana [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Congenital vitamin K-dependent coagulation factors deficiency [ORDO Disease]
MeSH Descriptor(s) used for indexing
- prothrombin [MeSH Descriptor]
Record concept(s)
- hypoprothrombinemias [MeSH concept]
Related MeSH Supplementary Concept(s)
- acquired hypoprothrombinemia [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Factor II Deficiency [NCIt concept]
- Factor II deficiency [MedDRA Preferred Term]
- Prothrombin deficiency, congenital [OMIM Phenotype]
- prothrombin deficiency [DO Concept]
Validated automatic mappings to BTNT
- Congenital factor II deficiency [ORDO Disease]
- blood clotting factor ii deficiency [Disease (Nov.)]

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