238099008: ApoA-I Munster variant 1 (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\ApoA-I Munster variant 1

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

356917012 ApoA-I Munster variant 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

626934010 ApoA-I Munster variant 1 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

5822651000241118 variante Munster 1 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

5822661000241115 variante Munster 1 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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
ApoA-I Munster variant 1	Is a	Apolipoprotein A-I variant disorder	true	Inferred relationship	Some
ApoA-I Munster variant 1	Occurrence	Congenital	false	Inferred relationship	Some
ApoA-I Munster variant 1	Finding site	Body system structure	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Description inactivation indicator reference set