238096001: Apolipoprotein A-I variant disorder (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Lipoprotein deficiency disorder\Apolipoprotein A-I variant disorder

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

356914017 Apolipoprotein A-I variant disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

626931019 Apolipoprotein A-I variant disorder (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356914017 Apolipoprotein A-I variant disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

626931019 Apolipoprotein A-I variant disorder (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5802561000241111 trouble d'une variante de l'apoA1 (apolipoprotéine A-I) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5802571000241115 trouble d'une variante de l'apolipoprotéine A-I fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5802561000241111 trouble d'une variante de l'apoA1 (apolipoprotéine A-I) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5802571000241115 trouble d'une variante de l'apolipoprotéine A-I fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Apolipoprotein A-I variant disorder	Is a	Lipoprotein deficiency disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Apolipoprotein A-I variant disorder	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Apolipoprotein A-I variant disorder	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Apo A-I Milano variant	Is a	True	Apolipoprotein A-I variant disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
Apo A-I Marburg variant (disorder)	Is a	True	Apolipoprotein A-I variant disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
ApoA-I Munster variant 1 (disorder)	Is a	True	Apolipoprotein A-I variant disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
ApoA-I Munster variant 2	Is a	True	Apolipoprotein A-I variant disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
ApoA-I Munster variant 3	Is a	True	Apolipoprotein A-I variant disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
Apo A-I Giessen variant	Is a	True	Apolipoprotein A-I variant disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
Apo A-I variant fisheye-like syndrome	Is a	True	Apolipoprotein A-I variant disorder	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets