717045004: Autosomal dominant hyperinsulinism due to Kir6.2 deficiency (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Finding of pancreas\Disorder of pancreas\Disorder of endocrine pancreas\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency

\Digestive system finding\Finding of pancreas\Disorder of pancreas\Disorder of endocrine pancreas\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of pancreas\Disorder of endocrine pancreas\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of pancreas\Disorder of endocrine pancreas\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Finding of pancreas\Disorder of pancreas\Disorder of endocrine pancreas\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of pancreas\Disorder of endocrine pancreas\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of pancreas\Disorder of endocrine pancreas\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of pancreas\Disorder of endocrine pancreas\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of pancreas\Disorder of endocrine pancreas\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of pancreas\Disorder of endocrine pancreas\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Disorder of glucose regulation\Hyperinsulinism\Autosomal dominant hyperinsulinism due to Kir6.2 deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3308264013 Autosomal dominant hyperinsulinism due to Kir6.2 deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

3308265014 Autosomal dominant hyperinsulinism due to Kir6.2 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency	Is a	Hyperinsulinism	true	Inferred relationship	Existential restriction modifier
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency	Is a	Hereditary disorder of endocrine system	true	Inferred relationship	Existential restriction modifier
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency	Finding site	Endocrine pancreatic structure	false	Inferred relationship	Existential restriction modifier
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	1
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency	Finding site	Endocrine pancreatic structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3308264013	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3308265014	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module