128204009: Hereditary motor and sensory neuropathy with retinitis pigmentosa (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary motor and sensory neuropathy with retinitis pigmentosa
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary motor and sensory neuropathy with retinitis pigmentosa
• \Disorder of body system\Neurological disorder\Neuropathy\Hereditary motor and sensory neuropathy with retinitis pigmentosa
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary motor and sensory neuropathy with retinitis pigmentosa
• \Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary motor and sensory neuropathy with retinitis pigmentosa

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1220787011	Hereditary motor-sensory neuropathy with retinitis pigmentosa	en	Synonym	Active	Case insensitive	SNOMED CT core
1220788018	Hereditary motor and sensory neuropathy type VII	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
206439010	Hereditary sensory-motor neuropathy, type VII	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
206440012	Hereditary motor and sensory neuropathy, type VII	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
206441011	HSMN VII	en	Synonym	Active	Case sensitive	SNOMED CT core
206442016	HMSN VII	en	Synonym	Active	Case sensitive	SNOMED CT core
206443014	Hereditary motor and sensory neuropathy with retinitis pigmentosa	en	Synonym	Active	Case insensitive	SNOMED CT core
732169018	Hereditary motor and sensory neuropathy with retinitis pigmentosa (disorder)	en	Fully specified name	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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