nephrotic syndrome type 9 (DOID:0080391)
Alliance: disease page
Alt IDs: OMIM:615573
Definition: A familial nephrotic syndrome characterized by steroid-resistant proteinuria, hypoalbuminemia and edema with onset in the first or second decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the COQ8B gene on chromosome 19q13.