familial nephrotic syndrome type-1 (Finnish congenital nephrosis, congenital nephrotic syndrome of the Finnish type)

Genetics

• autosomal recessive
• associated with defects in NPHS1

Clinical manifestations

• massive proteinuria in utero & nephrosis at birth

More general terms

• familial nephrotic syndrome

Database

• OMIM: https://mirror.omim.org/entry/256300