702419001: Fatty acid hydroxylase associated neurodegeneration (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of nervous system\Fatty acid hydroxylase associated neurodegeneration
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Fatty acid hydroxylase associated neurodegeneration
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Fatty acid hydroxylase associated neurodegeneration
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Fatty acid hydroxylase associated neurodegeneration
• \Disorder of body system\Neurological disorder\System disorder of the nervous system\Fatty acid hydroxylase associated neurodegeneration

Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2995450017	Fatty acid hydroxylase associated neurodegeneration (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2995568017	Fatty acid hydroxylase associated neurodegeneration	en	Synonym	Active	Case insensitive	SNOMED CT core
2995671015	Dysmyelinating leukodystrophy and spastic paraparesis	en	Synonym	Active	Case insensitive	SNOMED CT core
2995894016	Spastic paraplegia 35	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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