An instance of focal segmental glomerulosclerosis that is caused by an inherited genomic modification in an individual.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| HIV-associated nephropathy | MONDO:0005798 | ||
| Focal segmental glomerulosclerosis 1 | MONDO:0011303 | ACTN4 | |
| Focal segmental glomerulosclerosis 2 | MONDO:0011390 | TRPC6 | |
| Focal segmental glomerulosclerosis 5 | MONDO:0013191 | INF2 | |
| Focal segmental glomerulosclerosis 6 | MONDO:0013589 | MYO1E | |
| Focal segmental glomerulosclerosis 7 | MONDO:0014451 | PAX2 | |
| Focal segmental glomerulosclerosis 8 | MONDO:0014462 | ANLN | |
| Focal segmental glomerulosclerosis 9 | MONDO:0014539 | CRB2 | |
| Nail-patella-like renal disease | MONDO:0009724 | LMX1B |
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