33513003: Familial apolipoprotein C-II deficiency (disorder)

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

\Evaluation finding\Measurement finding\...

\Finding of substance level (finding)\Lipid level - finding\Lipids abnormal\Increased lipid\Hyperlipidemia\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridemia\Familial hyperchylomicronemia\Familial apolipoprotein C-II deficiency

\Measurement finding outside reference range\Measurement finding above reference range\Increased lipid\Hyperlipidemia\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridemia\Familial hyperchylomicronemia\Familial apolipoprotein C-II deficiency
\Measurement finding outside reference range\Lipids abnormal\Increased lipid\Hyperlipidemia\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridemia\Familial hyperchylomicronemia\Familial apolipoprotein C-II deficiency

\Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipoprotein storage and metabolism\Hyperlipidemia\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridemia\Familial hyperchylomicronemia\Familial apolipoprotein C-II deficiency

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

55921014 Familial apolipoprotein C-II deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
55922019 Apo-c-II deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
55923012 Anapolipoproteinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
485540016 Anapolipoproteinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
764927011 Familial apolipoprotein C-II deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
932431000052115 familjär apolipoprotein C-2-brist sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial apolipoprotein C-II deficiency	Is a	Familial hyperchylomicronemia	true	Inferred relationship	Some
Familial apolipoprotein C-II deficiency	Finding site	Body system structure	false	Inferred relationship	Some
Familial apolipoprotein C-II deficiency	Occurrence	Congenital	false	Inferred relationship	Some
Familial apolipoprotein C-II deficiency	Has definitional manifestation	Serum lipids high	false	Inferred relationship	Some
Familial apolipoprotein C-II deficiency	Has definitional manifestation	Increased lipid	false	Inferred relationship	Some
Familial apolipoprotein C-II deficiency	Interprets	Lipids measurement	true	Inferred relationship	Some	1
Familial apolipoprotein C-II deficiency	Has interpretation	Above reference range	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
familjär lipoproteinlipasbrist	Is a	False	Familial apolipoprotein C-II deficiency	Inferred relationship	Some

This concept is not in any reference sets