ODCs

Cytoscape Web

Click node...

Congenital analbuminemia

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Congenital nephrotic syndrome, Finnish type

1 OMIM reference -
1 associated gene
4 signs/symptoms

Congenital analbuminemia

Congenital nephrotic syndrome, Finnish type

(UniProt - OMIM)

(UniProt - OMIM)


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

Citations in the biomedical literature:

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

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive		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
Congenital analbuminemia
(no data available)