ODCs

Click node...

1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Congenital nephrotic syndrome, Finnish type

Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes


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

Citations in the biomedical literature:

Congenital nephrotic syndrome, Finnish type		Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes
	Synonym(s): - Finnish congenital nephrosis		Synonym(s): (no synonyms)

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

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

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