familial multiple coagulation factor deficiency I

Preferred Label : familial multiple coagulation factor deficiency I;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0565877;

UMLS CUI

C1856883;

Automatic exact mappings (from CISMeF team)
- Factor V and factor VIII, combined deficiency of, 1 [OMIM Phenotype]
Broader MeSH concept(s)
- Factor V And Factor VIII, Combined Deficiency Of [MeSH concept]
Related MeSH concept(s)
- Factor V And Factor VIII, Combined Deficiency Of, With Normal Protein C And Protein C Inhibitor [MeSH concept]
Related record
- familial multiple coagulation factor deficiency I [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Combined deficiency of factor V and factor VIII [ORDO Disease]
- Combined deficiency of factor V and factor VIII (disorder) [SNOMED CT concept]
- Factor V and factor VIII, combined deficiency of, 1 [OMIM Phenotype]
Validated automatic mappings to NTBT
- Combined deficiency of factor V and factor VIII [ORDO Disease]