Autosomal dominant hereditary disorder	Disorder of the central nervous system	Hereditary cancer-predisposing syndrome	Hereditary disorder of nervous system	Hereditary disorder of the integument	Neurocutaneous syndrome
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Tuberous sclerosis syndrome (disorder)
	Tuberous sclerosis syndrome
	Epiloia TS - Tuberous sclerosis Tuberous sclerosis Adenoma sebaceum syndrome Bourneville's disease
	tubereuze sclerose
	ziekte van Bourneville-Pringle
	tubereuze sclerose
	Dit is een syndroom met als kenmerken epilepsie, gezwelletjes in de huid, hersenen, nieren en longen, en een verstandelijke achterstand.

Id	7199000
Status	Primitive

Associated morphology	Neoplasm
Finding site	Structure of nervous system
Occurrence	Congenital

Associated morphology	Neoplasm
Finding site	Skin structure
Occurrence	Congenital

Associated morphology	Neoplasm and/or hamartoma
Finding site	Structure of central nervous system
Occurrence	Congenital

Associated morphology	Neoplasm and/or hamartoma
Finding site	Structure of multiple topographic sites
Occurrence	Congenital

PALGA thesaurus simple reference set for pathology

General Practice / Family Practice reference set

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q85.1
Rule	TRUE
Advice	ALWAYS Q85.1
Correlation	SNOMED CT source code to target map code correlation not specified

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Ash leaf spot, tuberous sclerosis

Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis

Fibrous skin tumor of tuberous sclerosis

Pulmonary tuberous sclerosis