dysfibrinogenemia, congenital - CISMeF

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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]

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03/05/2025

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