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783768006: Autosomal recessive hyperinsulinism due to Kir6.2 deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3760288013 Autosomal recessive hyperinsulinism due to Kir6.2 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3760289017 Autosomal recessive hyperinsulinism due to Kir6.2 deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3760290014 Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3760291013 Autosomal recessive hyperinsulinemic hypoglycaemia due to Kir6.2 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
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency Is a Hyperinsulinism true Inferred relationship Existential restriction modifier
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency Finding site Endocrine pancreatic structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive hyperinsulinism due to Kir6.2 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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