dysfibrinogenemia, congenital - CISMeF

" /> dysfibrinogenemia, congenital - CISMeF

CISMeF

chu

Dysfibrinogenemia, congenitalMeSH Supplementary Concept

Preferred Label : dysfibrinogenemia, congenital;

Details

Origin ID

C562727;

UMLS CUI

C0272350;

Automatic exact mappings (from CISMeF team)
- Congenital dysfibrinogenaemia [MedDRA Preferred Term]
- Congenital dysfibrinogenemia [MedDRA LLT]
- Dysfibrinogenemia, congenital [OMIM Phenotype]
- Hereditary dysfibrinogenemia (disorder) [SNOMED CT concept]
- congenital dysfibrinogenemia, nos [SNOMED Notion]
MeSH term(s) associated for indexing
- afibrinogenemia [MeSH Descriptor]
Record concept(s)
- dysfibrinogenemia, congenital [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital dysfibrinogenaemia [MedDRA Preferred Term]
- Congenital dysfibrinogenemia [MedDRA LLT]
- Dysfibrinogenemia, congenital [OMIM Phenotype]
- Familial dysfibrinogenemia [ORDO Disease]
- Familial hypodysfibrinogenemia [ORDO Disease]
- Hereditary dysfibrinogenemia (disorder) [SNOMED CT concept]
- congenital dysfibrinogenemia, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
22/05/2025

© Rouen University Hospital. Any partial or total use of this material must mention the source.