ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
4 signs/symptoms

Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis

Congenital nephrotic syndrome, Finnish type

APOL1	(UniProt - OMIM)		NPHS1	(UniProt - OMIM)
NPHS2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NPHS2	(0.95)	NPHS1

Citations in the biomedical literature:

Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis		Congenital nephrotic syndrome, Finnish type
	Synonym(s): - Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis		Synonym(s): - Finnish congenital nephrosis

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535761

Congenital nephrotic syndrome, Finnish type
	Very frequent - Autosomal recessive inheritance - Multicystic kidney / renal dysplasia - Nephrotic syndrome - Proteinuria
Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
(no data available)