heparin cofactor II deficiency

Preferred Label : heparin cofactor II deficiency;

MeSH note : mutation in HCF2;

MeSH synonym : hcf II deficiency; thrombophilia, susceptibility to, due to heparin cofactor ii deficiency;

Details

Origin ID

C562865;

UMLS CUI

C0398626;

Automatic exact mappings (from CISMeF team)
- Decreased level of heparin co-factor II [HPO term]
- heparin cofactor II deficiency [DO Concept]
Currated CISMeF NLP mapping
- Heparin cofactor II deficiency [OMIM Phenotype]
- Heparin cofactor II deficiency (disorder) [SNOMED CT concept]
- heparin cofactor 2 deficiency [Disease (Nov.)]
DO Cross reference
- heparin cofactor II deficiency [DO Concept]
MeSH term(s) associated for indexing
- heparin cofactor II [MeSH Descriptor]
- thrombosis [MeSH Descriptor]
Record concept(s)
- heparin cofactor II deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Heparin cofactor II deficiency [OMIM Phenotype]
- Heparin cofactor II deficiency [MedDRA Preferred Term]
- Heparin cofactor II deficiency (disorder) [SNOMED CT concept]
- heparin cofactor 2 deficiency [Disease (Nov.)]
- heparin cofactor II deficiency [DO Concept]

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