Factor VIII and factor ix, combined deficiency of

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

Symbol : F8F9D;

CISMeF acronym : FMFD II; F8F9D;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Familial multiple coagulation factor deficiency II; FMFD II;

Inheritance : Autosomal dominant;

Prefixed ID : 134510;

Details

Origin ID

134510;

UMLS CUI

C1851376;

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

Keyword's position in hierarchy(ies) :

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