Factor ix and factor XI, combined deficiency of

Preferred Label : Factor ix and factor XI, combined deficiency of;

CISMeF acronym : FMFD VI; MCFD6;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : FMFD VI; Multiple coagulation factor deficiency VI; MCFD6; Familial multiple coagulation factor deficiency VI;

Inheritance : ? Autosomal dominant;

Prefixed ID : 134540;

Details

Origin ID

134540;

UMLS CUI

C1851374;

Automatic exact mappings (from CISMeF team)
- familial multiple coagulation factor deficiency VI [MeSH concept]
- familial multiple coagulation factor deficiency VI [MeSH Supplementary Concept]
Broader ORDO disease(s)
- Hemophilia [ORDO Disease]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Reduced factor IX activity [HPO term]
- Reduced factor XI activity [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- familial multiple coagulation factor deficiency VI [MeSH Supplementary Concept]
- familial multiple coagulation factor deficiency VI [MeSH concept]

Keyword's position in hierarchy(ies) :

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