Autosomal dominant hereditary disorder	Congenital disorder of intestine	Congenital hamartoma	Congenital melanosis	Digestive system hereditary disorder	Hamartoma of intestine	Hereditary cancer-predisposing syndrome	Hereditary disorder of nervous system	Hereditary disorder of the integument	Intestinal polyposis syndrome	Lentiginosis	Neurocutaneous syndrome
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Peutz-Jeghers syndrome (disorder)
	Peutz-Jeghers syndrome
	PJS - Peutz-Jeghers syndrome Periorificial lentiginosis syndrome Peutz-Jeghers polyposis Perioral lentiginosis
	Peutz-Jeghers-syndroom
	syndroom van Peutz-Jeghers
	syndroom van Peutz-Jeghers
	PJS
	PJS; erfelijke aandoening met als kenmerken pigmentvlekken en darmpoliepen, met een verhoogde kans op kanker in het maag-darmkanaal en tumoren in de baarmoeder, eierstokken, borst en longen.

Id	54411001
Status	Defined

Associated morphology	Neoplasm
Finding site	Structure of nervous system
Occurrence	Congenital

Associated morphology	Peutz Jeghers polyp
Finding site	Intestinal structure
Occurrence	Congenital

Associated morphology	Neoplasm
Finding site	Skin structure
Occurrence	Congenital

Associated morphology	Lentigo
Finding site	Structure of skin and/or mucous membrane
Occurrence	Congenital

PALGA thesaurus simple reference set for pathology

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q85.8
Rule	TRUE
Advice	ALWAYS Q85.8
Correlation	SNOMED CT source code to target map code correlation not specified

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Peutz-Jeghers polyps of small bowel