Autosomal recessive hereditary disorder	Developmental hereditary disorder	Multiple malformation syndrome with unusual brain and/or neuromuscular findings
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Cohen syndrome (disorder)
	Cohen syndrome
	Cohen-syndroom
	syndroom van Cohen
	syndroom van Cohen
	Erfelijke aandoening met als belangrijkste kenmerken een kleine schedel, typisch gezicht, oogafwijkingen en slappe spieren.

Id	56604005
Status	Primitive

Associated morphology	Morphologically abnormal structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8
Correlation	SNOMED CT source code to target map code correlation not specified