ODCs

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3 OMIM references -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
3 associated genes
No signs/symptoms info

Familial progressive hyperpigmentation

Testicular seminomatous germ cell tumor

Citations in the biomedical literature:

Familial progressive hyperpigmentation		Testicular seminomatous germ cell tumor
	Synonym(s): - Melanosis diffusa congenita - Melanosis universalis hereditaria - Universal melanosis		Synonym(s): - Dysgerminoma of the testis - Dysgerminomatous germ cell tumor of the testis - Seminoma of the testis - Seminomatous germ cell tumor of the testis - Testicular dysgerminoma - Testicular dysgerminomatous germ cell tumor - Testicular seminoma

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

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

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: any age Type of inheritance: sporadic

	External references: 3 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.