Hyperproinsulinemia

Preferred Label : Hyperproinsulinemia;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the insulin gene (INS, 176730.0001);

Prefixed ID : #616214;

Details

Origin ID

616214;

UMLS CUI

C0342283;

CISMeF manual mappings
- hyperproinsulinemia [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Hyperproinsulinemia (disorder) [SNOMED CT concept]
- hyperproinsulinemia [Disease (Nov.)]
- hyperproinsulinemia [MeSH concept]
Genes related to phenotype
- Insulin [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hyperglycemia [HPO term]
- Hyperinsulinemia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperproinsulinemia (disorder) [SNOMED CT concept]
- hyperproinsulinemia [MeSH concept]
- hyperproinsulinemia [MeSH Supplementary Concept]
- hyperproinsulinemia [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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