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congenital nephrotic syndrome, Finnish type | RareConnect | RareConnect.io

/familial nephrotic syndrome

/congenital nephrotic syndrome, Finnish type

congenital nephrotic syndrome, Finnish type

Rare Disease

MONDO:0009732

Also Known As

Finnish congenital nephrosiscongenital nephrotic syndrome - Finnish typecongenital nephrotic syndrome, Finnish typenephrotic syndrome - NPHS1 associatedCnFNPHS1congenital nephrotic syndrome 1congenital nephrotic syndrome Finnish typenephrosis 1, congenital, Finnish typenephrosis, congenitalnephrotic syndrome, congenitalnephrotic syndrome, type 1

Definition

Congenital nephrotic syndrome, Finnish type is characterized by protein loss beginning during fetal life.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:256300 ↗

Orphanet

Orphanet:839 ↗

GARD

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