Autosomal dominant hyperinsulinism due to SUR1 deficiency 717046003
SNOMED CT code
SNOMED code | 717046003 |
---|---|
name | Autosomal dominant hyperinsulinism due to SUR1 deficiency |
status | active |
date introduced | 2016-07-31 |
fully specified name(s) | Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Endocrine pancreatic structure 78696007 |
parents | |
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 Autosomal dominant hyperinsulinism due to SUR1 deficiency 717046003 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Autosomal dominant hyperinsulinism due to SUR1 deficiency 717046003 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 Autosomal dominant hyperinsulinism due to SUR1 deficiency 717046003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Autosomal dominant hyperinsulinism due to SUR1 deficiency 717046003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of carbohydrate metabolism 20957000 Disorder of glucose regulation 237597000 Hyperinsulinism 83469008 Autosomal dominant hyperinsulinism due to SUR1 deficiency 717046003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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