ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation

Familial papillary renal cell carcinoma

NPHS1	(UniProt - OMIM)		MET	(UniProt - OMIM)
PTPRO	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PTPRO	(0.68)	MET

Citations in the biomedical literature:

Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation		Familial papillary renal cell carcinoma

	Classification (Orphanet): - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare genetic disease - Rare oncologic disease - Rare renal disease

	Classification (ICD10): - Diseases of the genitourinary system -		Classification (ICD10): - Neoplasms -

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

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C538614

No signs/symptoms info available.