OMOP Concept 36715529
Hyperinsulinism due to insulin receptor deficiency
StandardConditionSNOMED721235003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hyperinsulinism due to insulin receptor deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 721235003 | Hyperinsulinism due to insulin receptor deficiency | Non-standard |
Synonyms
Alternative names recorded for Hyperinsulinism due to insulin receptor deficiency across source vocabularies.
- hiperinsulinismo debido a deficiencia de receptor de insulina
- hiperinsulinismo debido a deficiencia de receptor de insulina (trastorno)
- Hyperinsulinism due to INSR (insulin receptor) deficiency
- Hyperinsulinism due to insulin receptor deficiency (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Digestive system hereditary disorder
- 1Familial hyperinsulinemic hypoglycemia
- 1Hereditary disorder of endocrine system
- 2Autosomal hereditary disorder
- 2Disorder of digestive system
- 2Disorder of endocrine system
- 2Familial disease
- 2Genetic disease
- 2Hereditary disorder by system
- 2Hyperinsulinism
- 2Hypoglycemic syndrome
- 3Digestive system finding
- 3Disease
- 3Disorder of body system
- 3Disorder of endocrine pancreas
- 3Disorder of glucose metabolism
- 3Disorder of glucose regulation
- 3Hereditary disease
- 4Clinical finding
- 4Disorder of carbohydrate metabolism
- 4Disorder of pancreas
- 5Disorder of digestive organ
- 5Disorder of retroperitoneum
- 5Finding of pancreas
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