Hyperinsulinism due to insulin receptor deficiency 721235003
SNOMED CT code
| SNOMED code | 721235003 |
|---|---|
| name | Hyperinsulinism due to insulin receptor deficiency |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Hyperinsulinism due to insulin receptor deficiency (disorder) |
| synonyms |
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| attributes - group2 | |
| Due to | Insulin receptor defect 10680005 |
| attributes - group1 | |
| Finding site | Endocrine pancreatic structure 78696007 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Hyperinsulinism due to insulin receptor deficiency 721235003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Familial disease 111941005 Familial hyperinsulinemic hypoglycemia 1296480005 Hyperinsulinism due to insulin receptor deficiency 721235003 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Hyperinsulinism due to insulin receptor deficiency 721235003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Hyperinsulinism due to insulin receptor deficiency 721235003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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