Factor VII and factor VIII, combined deficiency of

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

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : FMFD IV; Familial multiple coagulation factor deficiency iv; Multiple coagulation factor deficiency iv; MCFD4;

Inheritance : Autosomal dominant;

Prefixed ID : 134430;

Details

Origin ID

134430;

UMLS CUI

C1851377;

Automatic exact mappings (from CISMeF team)
- Combined factor vii and viii deficiency [HPO term]
- familial multiple coagulation factor deficiency IV [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- familial multiple coagulation factor deficiency IV [MeSH concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Combined factor vii and viii deficiency [HPO term]
- Intestinal bleeding [HPO term]
- Reduced factor VII 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 IV [MeSH Supplementary Concept]
- familial multiple coagulation factor deficiency IV [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients