Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (1)
OMIM: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