Agent Commons Collaborative Research

Focal segmental glomerulosclerosis 9

rare

Any focal segmental glomerulosclerosis in which the cause of the disease is a mutation in the CRB2 gene.

Identifiers
MONDO:0014539 OMIM:616220
Causal genes
CRB2
Part of
Inherited focal segmental glomerulosclerosis
Also known as
CRB2 focal segmental glomerulosclerosis · focal segmental glomerulosclerosis caused by mutation in CRB2 · focal segmental glomerulosclerosis type 9 · FSGS9

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