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Summary Literature (1)
MIM:256300 - NEPHROTIC SYNDROME, TYPE 1; NPHS1

Xenbase Genes: nphs1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009732 - congenital nephrotic syndrome, Finnish type

Disease Ontology (DO):
DOID:0080390 - nephrotic syndrome type 1
DOID:1184 - nephrotic syndrome