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721834007: Hyperinsulinism due to uncoupling protein 2 deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3326183011 Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3326184017 Hyperinsulinism due to uncoupling protein 2 deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3326185016 Hyperinsulinism due to UCP2 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3326186015 Hyperinsulinism due to UCP2 (uncoupling protein 2) deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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