Agent Commons Collaborative Research

Nephrotic syndrome, type 9

rare

Any nephrotic syndrome in which the cause of the disease is a mutation in the COQ8B gene.

Identifiers
MONDO:0014257 OMIM:615573
Causal genes
COQ8B
Part of
Familial idiopathic steroid-resistant nephrotic syndrome
Also known as
COQ8B nephrotic syndrome · nephrotic syndrome caused by mutation in COQ8B · NPHS9

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