Table 3.

Classification of CKD diagnoses in the CKiD Study, adapted from Warady et al., AJKD “Predictors of Rapid Progression of Glomerular and Non-glomerular Kidney Disease in Children and Adolescents: The Chronic Kidney Disease in Children (CKiD) Cohort”[13]

Glomerular	Non-glomerular
Chronic glomerulonephritis	Aplastic/hypoplastic/dysplastic kidneys
Congenital nephrotic syndrome	Autosomal dominant polycystic kidney disease
Denys-Drash syndrome	Autosomal recessive polycystic kidney disease
Familial nephritis	Branchio-oto-renal syndrome
Focal segmental glomerulosclerosis	Cystinosis
Hemolytic uremic syndrome	Medullary cystic disease/juvenile nephronophthisis
Henoch Schönlein nephritis	Obstructive uropathy
Idiopathic crescentic glomerulonephritis	Oxalosis
IgA nephropathy	Pyelonephritis/Interstitial nephritis
Membranoproliferative glomerulonephritis types I & II	Reflux nephropathy
Sickle cell nephropathy	Renal infarct
Systemic immunological disease (including SLE)	Syndrome of agenesis of abdominal musculature
	Wilms tumor