ODCs

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

COMMON GENES: 1

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

Familial progressive hyperpigmentation

Testicular non seminomatous germ cell tumor

KITLG	(UniProt - OMIM)		KITLG	(UniProt - OMIM)
			SPRY4	(UniProt - OMIM)

Citations in the biomedical literature:

Familial progressive hyperpigmentation		Testicular non seminomatous germ cell tumor
	Synonym(s): - Melanosis diffusa congenita - Melanosis universalis hereditaria - Universal melanosis		Synonym(s): - Non-seminomatous germ cell tumor of the testis - Testicular non-dysgerminomatous germ cell tumor - non-dysgerminomatous germ cell tumor of the testis

	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: (no data available)

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

No signs/symptoms info available.