ODCs

Click node...

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

COMMON GENES: 1

1 associated gene
No signs/symptoms info

Testicular non seminomatous germ cell tumor

Familial progressive hyper- and hypopigmentation

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

Citations in the biomedical literature:

Testicular non seminomatous germ cell tumor		Familial progressive hyper- and hypopigmentation
	Synonym(s): - Non-seminomatous germ cell tumor of the testis - Testicular non-dysgerminomatous germ cell tumor - non-dysgerminomatous germ cell tumor of the testis		Synonym(s): - FPHH

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.