protein c deficiency

Preferred Label : protein c deficiency;

MeSH definition : 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.);

MeSH synonym : protein c deficiencies; deficiency, protein c; deficiencies, protein c; hereditary thrombophilia due to protein C deficiency;

MeSH annotation : DF: PROTEIN C DEFIC;

Details

Origin ID

D020151;

UMLS CUI

C0398625;

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)
- Primary thrombophilia [ICD-10 Sub-category]
- Protein S deficiency [MedDRA Preferred Term]
- Protein deficiency [MedDRA Preferred Term]
- Protein z deficiency [OMIM Phenotype]
Currated CISMeF NLP mapping
- Protein C Deficiency Disease [NCIt concept]
- Protein C deficiency [PASCAL descriptor]
- Protein C deficiency [MedDRA Preferred Term]
- Protein C deficiency disease (disorder) [SNOMED CT concept]
- Reduced protein C activity [HPO term]
- protein C deficiency [Disease (Nov.)]
- protein C deficiency [DO Concept]
- protein c deficiency disease [SNOMED Notion]
DO Cross reference
- protein C deficiency [DO Concept]
HPO term
- Reduced protein C activity [HPO term]
MeSH Descriptor(s) used for indexing
- protein C [MeSH Descriptor]
Record concept(s)
- protein C deficiency [MeSH concept]
Related MeSH Supplementary Concept(s)
- congenital thrombotic disease, due to protein C deficiency [MeSH Supplementary Concept]
- protein C deficiency, acquired [MeSH Supplementary Concept]
- thrombophilia, hereditary, due to protein C deficiency, autosomal dominant [MeSH Supplementary Concept]
- thrombophilia, hereditary, due to protein C deficiency, autosomal recessive [MeSH Supplementary Concept]
See also
- activated protein c resistance [MeSH Descriptor]
See also (suggested by CISMeF)
- protein C [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Protein C Deficiency Disease [NCIt concept]
- Protein C deficiency [MedDRA Preferred Term]
- Protein C deficiency [PASCAL descriptor]
- Protein C deficiency disease (disorder) [SNOMED CT concept]
- Reduced protein C activity [HPO term]
- protein C deficiency [DO Concept]
- protein C deficiency [Disease (Nov.)]
- protein c deficiency disease [SNOMED Notion]

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