Hyperproglucagonemia

Preferred Label : Hyperproglucagonemia;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Glucagon, large molecular weight species of;

Inheritance : Autosomal dominant;

Prefixed ID : 145270;

Details

Origin ID

145270;

UMLS CUI

C1840388;

Currated CISMeF NLP mapping
- hyperproglucagonemia [MeSH concept]
- hyperproglucagonemia [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hyperproglucagonemia [MeSH Supplementary Concept]
- hyperproglucagonemia [MeSH concept]

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