familial multiple coagulation factor deficiency VI

Preferred Label : familial multiple coagulation factor deficiency VI;

MeSH synonym : MCFD6; factor IX and factor XI, combined deficiency; FMFD VI; multiple coagulation factor deficiency VI;

Details

Origin ID

C565022;

UMLS CUI

C1851374;

Automatic exact mappings (from CISMeF team)
- Factor ix and factor XI, combined deficiency of [OMIM Phenotype]
MeSH term(s) associated for indexing
- blood coagulation disorders, inherited [MeSH Descriptor]
Record concept(s)
- familial multiple coagulation factor deficiency VI [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Factor ix and factor XI, combined deficiency of [OMIM Phenotype]

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