Autosomal recessive hereditary disorder	Chronic nervous system disorder	Hereditary motor and sensory neuropathy
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Hereditary motor and sensory neuropathy with acrodystrophy (disorder)
	Hereditary motor and sensory neuropathy with acrodystrophy
	Autosomal recessive axonal Charcot-Marie-Tooth disease with acrodystrophy Autosomal recessive Charcot-Marie-Tooth type 2 with acrodystrophy
	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.
	hereditaire motorische en sensorische neuropathie met acrodystrofie
	autosomaal recessieve ziekte van Charcot-Marie-Tooth type 2 met acrodystrofie

Id	771144005
Status	Primitive

Clinical course

Finding site

Peripheral nervous system structure

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G60.0
Rule	TRUE
Advice	ALWAYS G60.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified