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Dyschromatosis symmetrica hereditaria

1 OMIM reference -
1 associated gene
5 signs/symptoms

PROTEIN INTERACTIONS: 1

Ovarian malignant Sertoli-Leydig cell tumor

1 associated gene
No signs/symptoms info

Dyschromatosis symmetrica hereditaria

Ovarian malignant Sertoli-Leydig cell tumor

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ADAR	(0.71)	DICER1

Citations in the biomedical literature:

Dyschromatosis symmetrica hereditaria		Ovarian malignant Sertoli-Leydig cell tumor
	Synonym(s): - Acropigmentation of Dohi		Synonym(s): - Androblastoma - Arrhenoblastoma - Ovarian Sertoli-Leydig cell cancer - Virilizing ovarian tumor

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare gynecologic or obstetric disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): - Neoplasms -

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

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

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
Ovarian malignant Sertoli-Leydig cell tumor
(no data available)