771144005: Hereditary motor and sensory neuropathy with acrodystrophy (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 acrodystrophy
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary motor and sensory neuropathy with acrodystrophy
• \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 acrodystrophy
• \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 acrodystrophy
• \Disorder of body system\Neurological disorder\Chronic nervous system disorder\Hereditary motor and sensory neuropathy with acrodystrophy
• \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 acrodystrophy
• \Chronic disease\Chronic nervous system disorder\Hereditary motor and sensory neuropathy with acrodystrophy

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3704561018	Autosomal recessive axonal Charcot-Marie-Tooth disease with acrodystrophy	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3704562013	Hereditary motor and sensory neuropathy with acrodystrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
3704563015	Hereditary motor and sensory neuropathy with acrodystrophy (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3704564014	Autosomal recessive Charcot-Marie-Tooth type 2 with acrodystrophy	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3703841011	A rare axonal hereditary motor and sensory neuropathy with characteristics of progressive axonal neuropathy with limb weakness and severe distal sensory loss in all limbs and acrodystrophic changes leading to painless non-healing ulcers, osteomyelitis, contractures and mutilating lesions with loss of terminal phalanges. One family with three affected siblings is described and there have been no further descriptions in the literature since 1999.	en	Definition	Active	Case sensitive	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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