congenital thrombotic disease, due to protein C deficiency

Preferred Label : congenital thrombotic disease, due to protein C deficiency;

MeSH synonym : PROC deficiency; thrombophilia, hereditary, due to pc deficiency;

Details

Origin ID

C535424;

UMLS CUI

C2930896;

Automatic exact mappings (from CISMeF team)
- Hereditary thrombophilia due to congenital protein C deficiency [ICD-11 More detail]
Currated CISMeF NLP mapping
- Severe hereditary thrombophilia due to congenital protein C deficiency [ORDO Disease]
MeSH term(s) associated for indexing
- protein c deficiency [MeSH Descriptor]
Record concept(s)
- Congenital thrombotic disease, due to Protein C deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Severe hereditary thrombophilia due to congenital protein C deficiency [ORDO Disease]

Keyword's position in hierarchy(ies) :

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