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1197489003: Familial chylomicronemia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4696546011 Familial chylomicronemia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4696547019 Familial chylomicronemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial chylomicronemia syndrome Is a Familial disease true Inferred relationship Existential restriction modifier
Familial chylomicronemia syndrome Is a Chylomicronemia syndrome true Inferred relationship Existential restriction modifier
Familial chylomicronemia syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Familial chylomicronemia syndrome Interprets Lipids measurement true Inferred relationship Existential restriction modifier 1
Familial chylomicronemia syndrome Has interpretation Above reference range true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial apolipoprotein C-II deficiency Is a True Familial chylomicronemia syndrome Inferred relationship Existential restriction modifier
Familial lipoprotein lipase deficiency Is a True Familial chylomicronemia syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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