vitamin K-Dependent clotting factors, combined deficiency of, 1

Preferred Label : vitamin K-Dependent clotting factors, combined deficiency of, 1;

MeSH note : mutation in GGCX;

MeSH synonym : familial multiple coagulation factor deficiency III; FMFD III; glutamic acid, deficient Gamma-Carboxylation of; multiple coagulation factor deficiency III; vitamin K-Dependent coagulation defect; VKCFD1; factors II, VII, IX, and X, combined deficiency of; MCFD3;

Details

Origin ID

C564741;

UMLS CUI

C1848534;

Currated CISMeF NLP mapping
- Vitamin k-dependent clotting factors, combined deficiency of, 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- blood coagulation disorders, inherited [MeSH Descriptor]
Record concept(s)
- vitamin K-Dependent clotting factors, combined deficiency of, 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary combined deficiency of vitamin K-dependent clotting factors [ORDO Disease]
- Vitamin k-dependent clotting factors, combined deficiency of, 1 [OMIM Phenotype]
- combined deficiency of vitamin K-dependent clotting factors 1 [DO Concept]
Validated automatic mappings to NTBT
- Hereditary combined deficiency of vitamin K-dependent clotting factors [ORDO Disease]
- Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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