hyperinsulinism, autosomal recessive

Preferred Label : hyperinsulinism, autosomal recessive;

MeSH note : Persistent hyperinsulinemic hypoglycemia of infancy due to focal adenomatous hyperplasia;

Details

Origin ID

C538567;

UMLS CUI

C2931886;

MeSH term(s) associated for indexing
- nesidioblastosis [MeSH Descriptor]
Record concept(s)
- Hyperinsulinism, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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