List of All Kidney Diseases

Here is the list of all Kidney Diseases

  1. 11-beta-hydroxylase deficiency
  2. 17-alpha-hydroxylase deficiency
  3. 17-beta hydroxysteroid dehydrogenase 3 deficiency
  4. 22q11.2 deletion syndrome
  5. 3-beta-hydroxysteroid dehydrogenase deficiency
  6. 46,XX testicular disorder of sex development
  7. 48,XXXY syndrome
  8. 48,XYYY
  9. 49, XXXXY syndrome
  10. 5-alpha reductase deficiency
  11. Aarskog syndrome
  12. Abruzzo-Erickson syndrome
  13. Acro-pectoro-renal field defect
  14. Acroosteolysis dominant type
  15. Acute intermittent porphyria
  16. Addison’s disease
  17. Adenine phosphoribosyltransferase deficiency
  18. Adrenocortical carcinoma
  19. Adult-onset Still’s disease
  20. ALG8-CDG (CDG-Ih)
  21. Allain-Babin-Demarquez syndrome
  22. Alpha-1 antitrypsin deficiency
  23. Alpha-thalassemia x-linked intellectual disability syndrome
  24. Alport syndrome
  25. Alström syndrome
  26. Amelogenesis imperfecta nephrocalcinosis
  27. Amyopathic dermatomyositis
  28. Aniridia renal agenesis psychomotor retardation
  29. Anorchia
  30. AREDYLD
  31. Aromatase deficiency
  32. Arthrogryposis renal dysfunction cholestasis syndrome
  33. Autosomal dominant distal renal tubular acidosis
  34. Autosomal dominant intermediate Charcot-Marie-Tooth disease type E – See Autosomal dominant intermediate Charcot-Marie-Tooth
  35. Autosomal dominant polycystic kidney disease – Not a rare disease
  36. Autosomal dominant pseudohypoaldosteronism type 1
  37. Autosomal dominant tubulointerstitial kidney disease
  38. Autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations
  39. Autosomal dominant tubulointerstitial kidney disease due to REN mutations
  40. Autosomal dominant tubulointerstitial kidney disease due to UMOD mutations
  41. Autosomal erythropoietic protoporphyria
  42. Autosomal recessive Alport syndrome
  43. Autosomal recessive polycystic kidney disease
  44. Autosomal recessive pseudohypoaldosteronism type 1
  45. Barakat syndrome
  46. Bardet-Biedl syndrome
  47. Bardet-Biedl syndrome 1
  48. Bardet-Biedl syndrome 10
  49. Bardet-Biedl syndrome 11
  50. Bardet-Biedl syndrome 12
  51. Bardet-Biedl syndrome 2
  52. Bartter syndrome type 3
  53. Bartter syndrome type 4
  54. Behçet disease
  55. Bifid nose with or without anorectal and renal anomalies
  56. Birt-Hogg-Dube syndrome
  57. BK-virus nephropathy
  58. Blue diaper syndrome
  59. Brachioskeletogenital syndrome
  60. Branchiootorenal syndrome
  61. Buerger disease
  62. Campomelic dysplasia
  63. Cat eye syndrome
  64. Caudal regression sequence
  65. CHARGE syndrome
  66. Chromosome 17q11.2 deletion syndrome
  67. Chromosome 8p23.1 deletion
  68. Collecting duct carcinoma
  69. Complete androgen insensitivity syndrome
  70. Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
  71. Congenital bilateral absence of the vas deferens
  72. Congenital erythropoietic porphyria
  73. Congenital nephrotic syndrome Finnish type
  74. Congenital thrombotic thrombocytopenic purpura
  75. Cranioectodermal dysplasia
  76. Crome syndrome
  77. Cystinosis
  78. Cystinuria
  79. Dandy-Walker cyst with Renal-Hepatic-Pancreatic dysplasia
  80. Dense deposit disease
  81. Dentatorubral-pallidoluysian atrophy
  82. Denys-Drash syndrome
  83. Dermatomyositis
  84. Diethylstilbestrol syndrome
  85. Diffuse cutaneous systemic sclerosis
  86. Dihydroxyadeninuria
  87. Diphallia
  88. Duplication of urethra
  89. Dyschondrosteosis nephritis
  90. EEC syndrome
  91. Ellis-Van Creveld syndrome
  92. Eosinophilic granulomatosis with polyangiitis
  93. Erythropoietic uroporphyria associated with myeloid malignancy
  94. Exstrophy of the bladder
  95. Fabry disease
  96. Faciocardiorenal syndrome
  97. Familial caudal dysgenesis
  98. Familial hyperthyroidism due to mutations in TSH receptor
  99. Familial LCAT deficiency
  100. Familial Mediterranean fever
  101. Familial prostate cancer
  102. Fanconi anemia
  103. Fanconi Bickel syndrome
  104. Fanconi syndrome
  105. Feigenbaum Bergeron Richardson syndrome
  106. Fibrillary glomerulonephritis
  107. Fibromuscular dysplasia – Not a rare disease
  108. Fish-eye disease
  109. Fitzsimmons Walson Mellor syndrome
  110. Focal segmental glomerulosclerosis
  111. Fowler’s syndrome
  112. Fraser syndrome
  113. Frasier syndrome
  114. Galactokinase deficiency
  115. Galloway-Mowat syndrome
  116. Genito palato cardiac syndrome
  117. Giant cell arteritis
  118. Gitelman syndrome
  119. Glomerulonephritis
  120. Glomerulopathy with fibronectin deposits 1
  121. Glomerulopathy with fibronectin deposits 2
  122. Glucocorticoid-remediable aldosteronism
  123. Glycogen storage disease type 1A
  124. Glycogen storage disease type 1B
  125. Goodpasture syndrome
  126. Graham Boyle Troxell syndrome
  127. Granulomatosis with polyangiitis
  128. Hartnup disease
  129. Henoch-Schonlein purpura
  130. Hepatoerythropoietic porphyria
  131. Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
  132. Hereditary coproporphyria
  133. Hereditary fructose intolerance
  134. Hereditary leiomyomatosis and renal cell cancer
  135. Hereditary paraganglioma-pheochromocytoma
  136. Hyperparathyroidism-jaw tumor syndrome
  137. Hypocomplementemic urticarial vasculitis
  138. Hypophosphatemic rickets
  139. Hypospadias familial
  140. Hypospadias-intellectual disability, Goldblatt type syndrome
  141. Hypotelorism cleft palate hypospadias
  142. Hypotrichosis-lymphedema-telangiectasia syndrome
  143. Ichthyosis-intellectual disability-dwarfism-renal impairment
  144. IgA nephropathy
  145. IMAGe syndrome
  146. Imerslund-Grasbeck syndrome
  147. Immunotactoid glomerulopathy
  148. Infundibulopelvic dysgenesis
  149. Interstitial cystitis – Not a rare disease
  150. Ivemark syndrome
  151. Jeune syndrome
  152. Joubert syndrome with oculorenal anomalies
  153. Juberg Marsidi syndrome
  154. Juvenile dermatomyositis
  155. Juvenile polymyositis
  156. Kawasaki disease
  157. Lesch Nyhan syndrome
  158. Liddle syndrome
  159. Limited cutaneous systemic sclerosis
  160. Limited systemic sclerosis
  161. Lowe oculocerebrorenal syndrome
  162. Lupus nephritis
  163. Male pseudohermaphroditism intellectual disability syndrome, Verloes type
  164. Maturity-onset diabetes of the young, type 5 – See Maturity-onset diabetes of the young
  165. Meacham Winn Culler syndrome
  166. Meckel syndrome
  167. Megacystis microcolon intestinal hypoperistalsis syndrome
  168. Membranous nephropathy
  169. Methylcobalamin deficiency cbl G type
  170. Methylmalonic acidemia
  171. Methylmalonic aciduria, cblA type – See Adenosylcobalamin deficiency
  172. Methylmalonic aciduria, cblB type – See Adenosylcobalamin deficiency
  173. Microscopic polyangiitis
  174. Minimal change disease
  175. Mixed connective tissue disease
  176. Muckle-Wells syndrome
  177. Multicentric carpotarsal osteolysis syndrome
  178. Multicystic renal dysplasia, bilateral
  179. Multisystemic smooth muscle dysfunction syndrome
  180. MURCS association
  181. Musculocontractural Ehlers-Danlos syndrome
  182. Naguib-Richieri-Costa syndrome
  183. Nail-patella syndrome
  184. Nephrocalcinosis
  185. Nephrogenic diabetes insipidus
  186. Nephrogenic diabetes insipidus-intracranial calcification-facial dysmorphism syndrome
  187. Nephronophthisis
  188. Neurofaciodigitorenal syndrome
  189. Noonan syndrome
  190. Noonan syndrome 1 – See Noonan syndrome
  191. Noonan syndrome 2 – See Noonan syndrome
  192. Noonan syndrome 3 – See Noonan syndrome
  193. Noonan syndrome 4 – See Noonan syndrome
  194. Noonan syndrome 5 – See Noonan syndrome
  195. Noonan syndrome 6 – See Noonan syndrome
  196. Ochoa syndrome
  197. Oculo skeletal renal syndrome
  198. Oligomeganephronic renal hypoplasia
  199. Omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects complex
  200. Orofaciodigital syndrome 1
  201. Osteopetrosis autosomal recessive 3
  202. PAGOD syndrome
  203. Pallister-Hall syndrome
  204. Papillary renal cell carcinoma
  205. Partial androgen insensitivity syndrome
  206. Perlman syndrome
  207. Perrault syndrome
  208. Persistent Müllerian duct syndrome
  209. Pheochromocytoma
  210. Pierson syndrome
  211. Polycystic kidney disease – Not a rare disease
  212. Polycystic kidneys, severe infantile with tuberous sclerosis
  213. Polyomavirus allograft nephropathy
  214. Porphyria cutanea tarda
  215. Postorgasmic illness syndrome
  216. Preaxial deficiency, postaxial polydactyly and hypospadias
  217. Primary hyperoxaluria type 1
  218. Primary hyperoxaluria type 2
  219. Primary hypomagnesemia with secondary hypocalcemia
  220. Proud syndrome
  221. Prune belly syndrome
  222. Pseudohypoaldosteronism type 2
  223. Pseudohypoparathyroidism type 1A
  224. Pseudohypoparathyroidism type 1B
  225. Pseudohypoparathyroidism type 1C
  226. Pseudohypoparathyroidism type 2
  227. Pseudopseudohypoparathyroidism
  228. Pseudoxanthoma elasticum
  229. Relapsing polychondritis
  230. Renal agenesis
  231. Renal coloboma syndrome
  232. Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia
  233. Renal dysplasia-limb defects syndrome
  234. Renal glycosuria
  235. Renal hypomagnesemia 2
  236. Renal hypomagnesemia-6
  237. Renal hypouricemia
  238. Renal medullary carcinoma
  239. Renal nutcracker syndrome
  240. Renal tubular acidosis with deafness
  241. Renal tubular dysgenesis
  242. Renal tubulopathy, diabetes mellitus, and cerebellar ataxia due to duplication of mitochondrial DNA
  243. Retinal vasculopathy with cerebral leukodystrophy with systemic manifestations
  244. Retroperitoneal fibrosis
  245. Reynolds syndrome
  246. RHYNS syndrome
  247. Saito Kuba Tsuruta syndrome
  248. Salcedo syndrome
  249. Sarcoidosis – Not a rare disease
  250. Schimke immunoosseous dysplasia
  251. Schinzel Giedion syndrome
  252. Senior Loken Syndrome
  253. SERKAL syndrome
  254. SeSAME syndrome
  255. Sickle beta thalassemia
  256. Sickle cell anemia
  257. Simpson-Golabi-Behmel syndrome
  258. Sirenomelia
  259. SLC35A1-CDG (CDG-IIf)
  260. Small cell carcinoma of the bladder
  261. Smith-Lemli-Opitz syndrome
  262. Split hand urinary anomalies spina bifida
  263. Spondyloepiphyseal dysplasia tarda X-linked
  264. Steinfeld syndrome
  265. Sudden infant death with dysgenesis of the testes syndrome
  266. Susac syndrome
  267. Swyer syndrome
  268. Takayasu arteritis
  269. Testicular seminoma
  270. Thin basement membrane nephropathy – Not a rare disease
  271. Thymic-Renal-Anal-Lung dysplasia
  272. Torticollis keloids cryptorchidism renal dysplasia
  273. Townes-Brocks syndrome
  274. Trisomy 13
  275. Trisomy 18
  276. Tuberous sclerosis complex
  277. Tubulointerstitial nephritis and uveitis
  278. Tyrosinemia type 1
  279. VACTERL association
  280. Variegate porphyria
  281. Von Hippel-Lindau disease
  282. WAGR syndrome
  283. Williams syndrome
  284. Wilms’ tumor
  285. Wilson disease
  286. X-linked hypophosphatemia
  287. X-linked lissencephaly with abnormal genitalia
  288. Xanthinuria type 1
  289. Xanthinuria type 2
  290. Zellweger syndrome

Source Link -: https://rarediseases.info.nih.gov/diseases/diseases-by-category/26/kidney-and-urinary-diseases