1187517009: Maternally inherited mitochondrial myopathy (disorder)

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

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy (disorder)\Mitochondrial myopathy (disorder)\Maternally inherited mitochondrial myopathy (disorder)

\Muscle finding (finding)\Disorder of muscle\...

\Disorder of skeletal muscle\Metabolic myopathy (disorder)\Mitochondrial myopathy (disorder)\Maternally inherited mitochondrial myopathy (disorder)

\Secondary myopathy\Maternally inherited mitochondrial myopathy (disorder)

\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\...

\Hereditary disorder of musculoskeletal system\Maternally inherited mitochondrial myopathy (disorder)

\Disorder of skeletal muscle\Metabolic myopathy (disorder)\Mitochondrial myopathy (disorder)\Maternally inherited mitochondrial myopathy (disorder)

\Disease\Genetic disease\Hereditary disease\Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder)\Maternally inherited mitochondrial myopathy (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Maternally inherited mitochondrial myopathy (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Maternally inherited mitochondrial myopathy (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Hereditary disorder of musculoskeletal system\Maternally inherited mitochondrial myopathy (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Metabolic myopathy (disorder)\Mitochondrial myopathy (disorder)\Maternally inherited mitochondrial myopathy (disorder)
\Disease\Disorder of muscle\Disorder of skeletal muscle\Metabolic myopathy (disorder)\Mitochondrial myopathy (disorder)\Maternally inherited mitochondrial myopathy (disorder)
\Disease\Disorder of muscle\Secondary myopathy\Maternally inherited mitochondrial myopathy (disorder)
\Disease\Metabolic disease\Mitochondrial cytopathy (disorder)\Mitochondrial myopathy (disorder)\Maternally inherited mitochondrial myopathy (disorder)
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy (disorder)\Mitochondrial myopathy (disorder)\Maternally inherited mitochondrial myopathy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Maternally inherited mitochondrial myopathy (disorder)	Is a	Mitochondrial myopathy (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Maternally inherited mitochondrial myopathy (disorder)	Due to	Mitochondrial cytopathy (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Maternally inherited mitochondrial myopathy (disorder)	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Maternally inherited mitochondrial myopathy (disorder)	Is a	Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Maternally inherited mitochondrial myopathy (disorder)	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Maternally inherited mitochondrial myopathy (disorder)	Is a	Secondary myopathy	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
4674063014	Maternally inherited mitochondrial myopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4674064015	Maternally inherited mitochondrial myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4674063014	Maternally inherited mitochondrial myopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4674064015	Maternally inherited mitochondrial myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6368361000241119	myopathie mitochondriale de transmission maternelle	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6368371000241110	myopathie mitochondriale héritée de la mère	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6368361000241119	myopathie mitochondriale de transmission maternelle	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6368371000241110	myopathie mitochondriale héritée de la mère	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module