intrinsic factor and R binder, combined congenital deficiency of

Preferred Label : intrinsic factor and R binder, combined congenital deficiency of;

Origin ID

C565461;

UMLS CUI

C1855721;

Currated CISMeF NLP mapping
- Intrinsic factor and r binder, combined congenital deficiency of [OMIM Phenotype]
MeSH term(s) associated for indexing
- intrinsic factor [MeSH Descriptor]
- metabolism, inborn errors [MeSH Descriptor]
- transcobalamins [MeSH Descriptor]
Record concept(s)
- intrinsic factor and R binder, combined congenital deficiency of [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Intrinsic factor and r binder, combined congenital deficiency of [OMIM Phenotype]