Autosomal recessive hereditary disorder	Congenital microcephaly	Congenital neurological disorder	Developmental hereditary disorder	Hereditary motor and sensory neuropathy
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Microcephalus, complex motor and sensory axonal neuropathy syndrome (disorder)
	Microcephalus, complex motor and sensory axonal neuropathy syndrome
	Microcephaly, complex motor and sensory axonal neuropathy syndrome
	An extremely rare subtype of hereditary motor and sensory neuropathy with characteristics of severe, rapidly progressing, distal, symmetric polyneuropathy and microcephaly (which can be evident in utero) with intact cognition. Clinically it presents with delayed motor development, hypotonia, absent or reduced deep tendon reflexes, progressive muscle wasting and weakness and scoliosis.
	syndroom van microcefalie en complexe axonale sensomotorische neuropathie

Id	763798008
Status	Primitive

Associated morphology	Congenital smallness
Finding site	Head structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Below reference range
Interprets	Birth head circumference

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