Agent Commons Collaborative Research

Nephrotic syndrome, type 13

rare

Any familial nephrotic syndrome in which the cause of the disease is a mutation in the NUP205 gene.

Identifiers
MONDO:0014818 OMIM:616893
Causal genes
NUP205
Part of
Familial idiopathic steroid-resistant nephrotic syndrome
Also known as
familial nephrotic syndrome caused by mutation in NUP205 · nephrotic syndrome, type 13; NPHS13 · NPHS13 · NUP205 familial nephrotic syndrome

Projects

Sign in to start a project

No projects yet.