123762005: Hypoinsulinism (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Abdominal organ finding\Finding of pancreas\Disorder of pancreas\Disorder of endocrine pancreas\Hypoinsulinism

\Digestive system finding (finding)\Finding of pancreas\Disorder of pancreas\Disorder of endocrine pancreas\Hypoinsulinism
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of pancreas\Disorder of endocrine pancreas\Hypoinsulinism

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

192251014 Hypoinsulinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

726829013 Hypoinsulinism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1289061000005110 Hypoinsulinisme da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hypoinsulinism	Is a	Hyperglycemic disorder	false	Inferred relationship	Some
Hypoinsulinism	Is a	Disorder of endocrine pancreas	true	Inferred relationship	Some
Hypoinsulinism	Finding site	Endocrine pancreatic structure	true	Inferred relationship	Some	1
Hypoinsulinism	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
Hypoinsulinism	Finding site	Structure of digestive system (body structure)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Post-surgical hypoinsulinemia	Is a	False	Hypoinsulinism	Inferred relationship	Some
Hypoinsulinemia following procedure (disorder)	Is a	True	Hypoinsulinism	Inferred relationship	Some
A rare genetic endocrine disease characterized by neonatal macrosomia, asymmetrical overgrowth (typically manifesting as left-sided hemihypertrophy) and recurrent, severe hypoinsulinemic (or hypo ketotic hypo-fatty-acidemic) hypoglycemia in infancy, which results in episodes of reduced consciousness and seizures. There is evidence the disease can be caused by heterozygous mutation in the AKT2 gene on chromosome 19q13.	Is a	True	Hypoinsulinism	Inferred relationship	Some

This concept is not in any reference sets