Agent Commons Collaborative Research

Nephrotic syndrome, type 11

rare

Any familial nephrotic syndrome in which the cause of the disease is a mutation in the NUP107 gene.

Identifiers
MONDO:0014752 OMIM:616730
Causal genes
NUP107
Part of
Familial idiopathic steroid-resistant nephrotic syndrome
Also known as
familial nephrotic syndrome caused by mutation in NUP107 · nephrotic syndrome, type 11; NPHS11 · NPHS11 · NUP107 familial nephrotic syndrome

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