1187520001: Leigh syndrome due to cytochrome C oxidase deficiency (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Disorder of brain\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency
\Central nervous system finding\Disorder of the central nervous system\Central nervous system complication\Leigh syndrome due to cytochrome C oxidase deficiency
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency
\Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency

\Finding of head and neck region\Head finding\...

\Finding of brain\Disorder of brain\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency

\Disorder of head\Disorder of brain\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency
\Disease\Disorder of body system\Disorder of nervous system\System disorder of the nervous system\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Central nervous system complication\Leigh syndrome due to cytochrome C oxidase deficiency
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency
\Disease\Disorder of head\Disorder of brain\Leigh's disease\Leigh syndrome due to cytochrome C oxidase deficiency

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

4674069013 Leigh syndrome due to cytochrome C oxidase deficiency (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

4674070014 Leigh syndrome due to cytochrome C oxidase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Leigh syndrome due to cytochrome C oxidase deficiency	Is a	Leigh's disease	true	Inferred relationship	Existential restriction modifier
Leigh syndrome due to cytochrome C oxidase deficiency	Is a	Central nervous system complication	true	Inferred relationship	Existential restriction modifier
Leigh syndrome due to cytochrome C oxidase deficiency	Due to	Cytochrome-c oxidase deficiency	true	Inferred relationship	Existential restriction modifier	1
Leigh syndrome due to cytochrome C oxidase deficiency	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier	2
Leigh syndrome due to cytochrome C oxidase deficiency	Associated morphology	Degenerative abnormality	true	Inferred relationship	Existential restriction modifier	2

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
4674069013	Leigh syndrome due to cytochrome C oxidase deficiency (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
4674070014	Leigh syndrome due to cytochrome C oxidase deficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module