ODCs

Cytoscape Web

Click node...

Congenital nephrotic syndrome, Finnish type

1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

Congenital analbuminemia

1 associated gene
No signs/symptoms info

Congenital nephrotic syndrome, Finnish type

Congenital analbuminemia

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NPHS1	(0.72)	ALB

Citations in the biomedical literature:

Congenital nephrotic syndrome, Finnish type		Congenital analbuminemia
	Synonym(s): - Finnish congenital nephrosis		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Diseases of the genitourinary system -		Classification (ICD10): - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

	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
Congenital analbuminemia
(no data available)