49973006: Familial lipoprotein deficiency (disorder)

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

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

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

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

83235013 Familial lipoprotein deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

787710013 Familial lipoprotein deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

83235013 Familial lipoprotein deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

83235013 Familial lipoprotein deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

83238010 Familial hypolipoproteinemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

495557015 Familial hypolipoproteinaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

787710013 Familial lipoprotein deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

787710013 Familial lipoprotein deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4553151000241113 déficit familial en lipoprotéines fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4553151000241113 déficit familial en lipoprotéines fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial lipoprotein deficiency	Is a	Inborn error of lipoprotein metabolism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial lipoprotein deficiency	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial lipoprotein deficiency	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial hypoalphalipoproteinemia	Is a	True	Familial lipoprotein deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial hypobetalipoproteinaemia	Is a	True	Familial lipoprotein deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)
Tangier disease (disorder)	Is a	True	Familial lipoprotein deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets