has material basis in germline mutation in NPHS1 familial nephrotic syndrome nephrotic syndrome congenital nephrotic syndrome, Finnish type https://rarediseases.info.nih.gov/diseases/1500/congenital-nephrotic-syndrome-finnish-type https://www.malacards.org/card/nephrotic_syndrome_type_1 nephrotic syndrome, type 1 SCTID:197601003 MONDO:0009732 congenital nephrotic syndrome - Finnish type DOID:0080390 NPHS1 nephrosis 1, congenital, Finnish type congenital nephrotic syndrome Finnish type congenital nephrotic syndrome, Finnish type Finnish congenital nephrosis MEDGEN:98011 CnF congenital nephrotic syndrome 1 nephrotic syndrome - NPHS1 associated Congenital nephrotic syndrome, Finnish type is characterized by protein loss beginning during fetal life. nephrosis, congenital MedDRA:10060740 NANDO:2200110 NCIT:C122795 OMIM:256300 GARD:0001500 UMLS:C0403399 Orphanet:839