Data current at May 2025.

You may also wish to refer to:

 

Rare Disease Group Cohort Size Lab results via data feed Patients recorded as being on RRT Number of patients with Creatinine readings Mean number of Creatinine readings per patient
Alport Syndrome 1200 901 434 991 87
APRT Deficiency 10 7 2 9 75
Atypical Haemolytic Uraemic Syndrome 317 257 156 266 165
Autosomal Dominant Polycystic Kidney Disease 9065 7416 3674 7859 94
Autosomal Dominant Tubulointerstitial Kidney Disease (FUAN) 268 210 120 218 98
Autosomal Recessive Polycystic Kidney Disease/Nephronophthisis 275 224 122 244 117
BK Nephropathy 153 143 140 143 384
Calciphylaxis 74 60 62 60 281
CKD due to Genetic Factors in people of African ancestry 636 232 139 231 148
CMV Post Transplant 647 562 576 582 307
Congenital Anomalies of the Kidneys and Urinary Tracts 384 237 61 282 76
Cystinosis 196 168 110 173 166
Cystinuria 537 352 10 393 29
Dent Disease and Lowe Syndrome 78 45 17 50 74
Fabry Disease 64 52 27 55 97
Fibromuscular Dysplasia 100 55 0 59 14
HNF1b Mutations 126 85 19 96 45
Hyperoxaluria 145 116 43 119 87
Idiopathic Nephrotic Syndrome 5020 3699 1200 4233 89
IgA Nephropathy 5309 4434 2634 4587 124
Inherited Renal Cancer Syndromes 426 20 4 82 20
Lupus Nephritis 183 107 8 119 77
Membranoproliferative Glomerulonephritis 1273 1024 640 1168 138
Membranous Nephropathy 2950 2233 607 2396 84
Mitochondrial Renal Disease 6 2 0 2 79
Monoclonal Gammopathy of Renal Significance 267 201 113 205 136
Pregnancy 812 633 253 715 110
Pure Red Cell Aplasia 9 6 6 6 240
Retroperitoneal Fibrosis 171 115 22 133 73
STEC-associated HUS 193 118 83 127 57
Tuberous Sclerosis 301 210 22 219 43
Tubulopathy 467 290 17 340 44
Vasculitis 5829 3974 1243 4300 92