73782007: congenitale myopathie met sterk vergrote mitochondriën (aandoening)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

122534014 Megaconial myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

122535010 Pleoconial myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

814208012 Megaconial myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

10613661000146115 congenitale myopathie met sterk vergrote mitochondriën nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

10613671000146114 congenitale musculaire dystrofie met sterk vergrote mitochondriën nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

10613681000146111 congenitale myopathie met sterk vergrote mitochondriën (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

10613691000146113 megaconial myopathy nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

12812651000146114 congenitale musculaire dystrofie door fosfatidylcholinebiosynthesedefect nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
congenitale myopathie met sterk vergrote mitochondriën	Is a	Myopathy	false	Inferred relationship	Some
congenitale myopathie met sterk vergrote mitochondriën	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
congenitale myopathie met sterk vergrote mitochondriën	Is a	Disorder of skeletal muscle	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)