Autosomal dominant hereditary disorder	Congenital hamartoma of skin	Developmental hereditary disorder	Hereditary cancer-predisposing syndrome	Hereditary disorder of the integument	Multiple malformation syndrome with early overgrowth
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PTEN hamartoma tumor syndrome (disorder)
	PTEN hamartoma tumor syndrome
	A term defining a group of clinically heterogeneous disorders united by a germline PTEN mutation and the involvement of derivatives of all 3 germ cell layers, manifesting with hamartomas, overgrowth and neoplasia. Disease onset depends on the specific disorder. The most important component seen in this group are malignancies.
	PTEN-hamartoom-tumorsyndroom
	PHTS
	PTEN-hamartoom-tumorsyndroom
	PHTS; zeldzame, erfelijke aandoening met als kenmerken een groter hoofd, gezwelletjes op gezicht, handen, voeten en in diverse organen en een verhoogde kans op goed- of kwaadaardige tumoren, bij vrouwen met name in de borst of baarmoeder.

Id	722859001
Status	Primitive

Associated morphology	Hamartoma
Finding site	Skin structure
Occurrence	Congenital

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

ICD-10 complex map reference set

Target	Q85.8
Rule	TRUE
Advice	ALWAYS Q85.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

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Bannayan syndrome

Cowden syndrome

Proteus like syndrome

Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome