709415008: Mitochondrial membrane protein associated neurodegeneration (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of nervous system\Mitochondrial membrane protein associated neurodegeneration
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Mitochondrial membrane protein associated neurodegeneration
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Mitochondrial membrane protein associated neurodegeneration
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Mitochondrial membrane protein associated neurodegeneration

Status: current, Primitive. Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3039919013	Mitochondrial membrane protein associated neurodegeneration (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3040079012	Mitochondrial membrane protein associated neurodegeneration	en	Synonym	Active	Case insensitive	SNOMED CT core
3078351015	Neurodegeneration with brain iron accumulation 4	en	Synonym	Active	Case insensitive	SNOMED CT core
3078599019	Mitochondrial protein associated neurodegeneration	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Strength reference set

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