49973006: Familial lipoprotein deficiency (disorder)

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

\Genetic disease\Hereditary disease\Inborn error of metabolism\Familial lipoprotein deficiency

\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Familial lipoprotein deficiency

\Metabolic disease\Inborn error of metabolism\Familial lipoprotein deficiency
\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Familial lipoprotein deficiency

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: IPS terminology module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

83235013 Familial lipoprotein deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)

787710013 Familial lipoprotein deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial lipoprotein deficiency	Is a	Disorder of lipoprotein AND/OR lipid metabolism	true	Inferred relationship	Some
Familial lipoprotein deficiency	Is a	Inborn error of metabolism	true	Inferred relationship	Some
Familial lipoprotein deficiency	Occurrence	Congenital	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial hypoalphalipoproteinemia	Is a	True	Familial lipoprotein deficiency	Inferred relationship	Some

This concept is not in any reference sets