X-linked hereditary motor and sensory neuropathy	X-linked recessive hereditary disease
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X-linked Charcot-Marie-Tooth disease type 2 (disorder)
	X-linked Charcot-Marie-Tooth disease type 2
	A rare genetic peripheral sensorimotor neuropathy with an X-linked recessive inheritance pattern and the infantile to childhood-onset of progressive, distal muscle weakness and atrophy (more prominent in the lower extremities than in the upper extremities), pes cavus, and absent tendon reflexes. Sensory impairment and intellectual disability has been reported in some individuals.
	X-gebonden hereditaire motorisch-sensibele neuropathie type 2
	CMT2X X-gebonden HMSN type 2 X-gebonden HMSN van axonaal type X-gebonden hereditaire motorisch-sensorische neuropathie type 2 X-gebonden ziekte van Charcot-Marie-Tooth type 2

Id	763457000
Status	Primitive

Finding site	Peripheral nervous system structure
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G60.0
Rule	TRUE
Advice	ALWAYS G60.0
Correlation	SNOMED CT source code to target map code correlation not specified