insulin receptor, defect in

Preferred Label : insulin receptor, defect in;

MeSH note : mutation in INSR;

Origin ID

C562709;

UMLS CUI

C0271689;

Automatic exact mappings (from CISMeF team)
- Donohue syndrome [OMIM Phenotype]
- Insulin receptor defect (disorder) [SNOMED CT concept]
- insulin receptor defect, nos [SNOMED Notion]
MeSH term(s) associated for indexing
- donohue syndrome [MeSH Descriptor]
Record concept(s)
- insulin receptor, defect in [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Insulin receptor defect (disorder) [SNOMED CT concept]
- insulin receptor defect, nos [SNOMED Notion]