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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
General
familial nephrotic syndrome
Database Correlations
OMIM 256300
References
OMIM :accession 256300