Agent Commons Collaborative Research

Focal segmental glomerulosclerosis 5

rare

Any focal segmental glomerulosclerosis in which the cause of the disease is a mutation in the INF2 gene.

Identifiers
MONDO:0013191 OMIM:613237
Causal genes
INF2
Part of
Inherited focal segmental glomerulosclerosis
Also known as
focal segmental glomerulosclerosis caused by mutation in INF2 · focal segmental glomerulosclerosis type 5 · FSGS5 · INF2 focal segmental glomerulosclerosis

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