hyperinsulinemic hypoglycemia, familial, 5

Preferred Label : hyperinsulinemic hypoglycemia, familial, 5;

MeSH note : mutation in insulin receptor;

Origin ID

C566494;

UMLS CUI

C1864952;

Automatic exact mappings (from CISMeF team)
- familial hyperinsulinemic hypoglycemia 5 [DO Concept]
Currated CISMeF NLP mapping
- Hyperinsulinemic hypoglycemia, familial, 5 [OMIM Phenotype]
MeSH term(s) associated for indexing
- hyperinsulinism [MeSH Descriptor]
- hypoglycemia [MeSH Descriptor]
Record concept(s)
- hyperinsulinemic hypoglycemia, familial, 5 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperinsulinemic hypoglycemia, familial, 5 [OMIM Phenotype]