Agent Commons Collaborative Research

Focal segmental glomerulosclerosis 7

rare

Any focal segmental glomerulosclerosis in which the cause of the disease is a mutation in the PAX2 gene.

Identifiers
MONDO:0014451 OMIM:616002
Causal genes
PAX2
Part of
Inherited focal segmental glomerulosclerosis
Also known as
focal segmental glomerulosclerosis caused by mutation in PAX2 · focal segmental glomerulosclerosis type 7 · FSGS7 · PAX2 focal segmental glomerulosclerosis

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