Data current August 2025.

You may also wish to refer to:

Rare Disease Group Cohort Size Lab results via data feed Patients recorded as being on KRT Number of patients with Creatinine readings Mean number of Creatinine readings per patient
Alport Syndrome 1246 938 440 1056 90
APRT Deficiency 10 7 2 9 75
Atypical Haemolytic Uraemic Syndrome 341 274 162 283 172
Autosomal Dominant Polycystic Kidney Disease 9174 7575 3688 8010 96
Autosomal Dominant Tubulointerstitial Kidney Disease (FUAN) 272 215 120 223 98
Autosomal Recessive Polycystic Kidney Disease/Nephronophthisis 277 225 124 246 120
BK Nephropathy 175 164 148 164 361
Calciphylaxis 78 67 63 67 284
CKD due to Genetic Factors in people of African ancestry 689 252 161 253 146
CMV Post Transplant 697 615 676 651 307
Congenital Anomalies of the Kidneys and Urinary Tracts 430 261 66 315 76
Cystinosis 200 173 110 178 174
Cystinuria 541 361 10 399 30
Dent Disease and Lowe Syndrome 82 48 17 53 74
Fabry Disease 65 54 27 57 103
Fibromuscular Dysplasia 108 65 0 64 15
HNF1b Mutations 130 91 21 98 50
Hyperoxaluria 145 118 43 122 93
Idiopathic Nephrotic Syndrome 5085 3781 1205 4313 91
IgA Nephropathy 5398 4541 2641 4693 125
Inherited Renal Cancer Syndromes 448 22 4 84 20
Lupus Nephritis 273 163 10 177 79
Membranoproliferative Glomerulonephritis 1285 1047 643 1189 140
Membranous Nephropathy 2994 2291 608 2455 85
Mitochondrial Renal Disease 6 2 0 2 79
Monoclonal Gammopathy of Renal Significance 273 209 114 213 137
Pregnancy 825 644 257 731 113
Pure Red Cell Aplasia 9 6 6 6 241
Retroperitoneal Fibrosis 175 120 22 138 72
STEC-associated HUS 201 121 86 133 57
Tuberous Sclerosis 304 213 22 222 44
Tubulopathy 491 313 17 364 43
Vasculitis 5908 4135 1245 4458 91