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Peripheral primitive neuroectodermal tumor

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Dyschromatosis symmetrica hereditaria

1 OMIM reference -
1 associated gene
5 signs/symptoms

Peripheral primitive neuroectodermal tumor

Dyschromatosis symmetrica hereditaria

ERG	(UniProt - OMIM)		ADAR	(UniProt - OMIM)
FLI1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ERG	(0.68)	ADAR

Citations in the biomedical literature:

Peripheral primitive neuroectodermal tumor		Dyschromatosis symmetrica hereditaria
	Synonym(s): - PPNET - Peripheral PNET		Synonym(s): - Acropigmentation of Dohi

	Classification (Orphanet): - Rare bone disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the skin and subcutaneous tissue -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535729

Dyschromatosis symmetrica hereditaria
	Very frequent - Irregular / in bands / reticular skin hyperpigmentation - Irregular / patchy skin hypopigmentation - Macules Frequent - Autosomal recessive inheritance - Dystonia / torticollis / writer's cramp / blepharospasms
Peripheral primitive neuroectodermal tumor
(no data available)