thrombophilia, hereditary, due to protein C deficiency, autosomal dominant

Preferred Label : thrombophilia, hereditary, due to protein C deficiency, autosomal dominant;

MeSH synonym : protein C deficiency, autosomal dominant; PROC deficiency, autosomal dominant;

Détails

Origin ID

C567163;

UMLS CUI

C2674321;

Automatic exact mappings (from CISMeF team)
- Thrombophilia due to protein C deficiency, autosomal dominant [OMIM Phenotype]
- autosomal dominant thrombophilia due to protein C deficiency [DO Concept]
DO Cross reference
- autosomal dominant thrombophilia due to protein C deficiency [DO Concept]
MeSH term(s) associated for indexing
- protein c deficiency [MeSH Descriptor]
Record concept(s)
- thrombophilia, hereditary, due to protein C deficiency, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Thrombophilia due to protein C deficiency, autosomal dominant [OMIM Phenotype]
- autosomal dominant thrombophilia due to protein C deficiency [DO Concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients