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Orphanet classification of rare transplant-related disorders

Rare disorder potentially indicated for transplant or complication after transplantation ORPHA:565779
- Rare disorder potentially indicated for transplant ORPHA:506207
  - Rare disorder potentially indicated for kidney transplant ORPHA:506213
    - 46,XX gonadal dysgenesis ORPHA:243
    - 46,XX ovotesticular disorder of sex development ORPHA:2138
    - 46,XX testicular disorder of sex development ORPHA:393
    - 46,XY complete gonadal dysgenesis ORPHA:242
    - 46,XY disorder of sex development due to impaired androgen production ORPHA:325357
    - 46,XY disorder of sex development induced by maternal exposure to endocrine disruptors ORPHA:325537
    - 46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome ORPHA:168563
    - 46,XY ovotesticular disorder of sex development ORPHA:325345
    - 46,XY partial gonadal dysgenesis ORPHA:251510
    - Acquired monoclonal Ig light chain-associated Fanconi syndrome ORPHA:91136
    - Adenine phosphoribosyltransferase deficiency ORPHA:976
    - Adult familial nephronophthisis-spastic quadriparesia syndrome ORPHA:2666
    - Alström syndrome ORPHA:64
    - Apparent mineralocorticoid excess ORPHA:320
    - Atypical Fanconi syndrome-neonatal hyperinsulinism syndrome ORPHA:544628
    - Autosomal dominant polycystic kidney disease ORPHA:730
    - Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis ORPHA:88924
    - Autosomal dominant progressive nephropathy with hypertension ORPHA:88659
    - Autosomal dominant tubulointerstitial kidney disease ORPHA:34149
    - Autosomal recessive infantile hypercalcemia ORPHA:300547
    - Autosomal recessive polycystic kidney disease ORPHA:731
    - Bardet-Biedl syndrome ORPHA:110
    - Bartter syndrome type 1 ORPHA:620217
    - Bartter syndrome type 2 ORPHA:620220
    - Bartter syndrome type 3 ORPHA:93605
    - Bartter syndrome type 4 ORPHA:89938
    - Brachydactyly-arterial hypertension syndrome ORPHA:1276
    - Cataract-nephropathy-encephalopathy syndrome ORPHA:1380
    - Clear cell sarcoma of kidney ORPHA:457246
    - Congenital mesoblastic nephroma ORPHA:2665
    - Congenital renal artery stenosis ORPHA:97598
    - Cranioectodermal dysplasia ORPHA:1515
    - Cystinuria ORPHA:214
    - Dent disease ORPHA:1652
    - Distal renal tubular acidosis ORPHA:18
    - Dominant hypophosphatemia with nephrolithiasis or osteoporosis ORPHA:244305
    - Enamel-renal syndrome ORPHA:1031
    - Fabry disease ORPHA:324
    - Familial hyperaldosteronism ORPHA:235936
    - Familial hyperthyroidism due to mutations in TSH receptor ORPHA:424
    - Fanconi anemia ORPHA:84
    - Full NF2-related schwannomatosis ORPHA:637
    - Full schwannomatosis ORPHA:93921
    - Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation ORPHA:620371
    - Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome ORPHA:404476
    - Glomerular disease ORPHA:93548
    - Hemolytic uremic syndrome ORPHA:544458
    - Hepatic fibrosis-renal cysts-intellectual disability syndrome ORPHA:2031
    - Hereditary renal hypouricemia ORPHA:94088
    - Hypertension due to gain-of-function mutations in the mineralocorticoid receptor ORPHA:88660
    - Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome ORPHA:363694
    - Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome ORPHA:528105
    - Hypotonia-cystinuria type 1 syndrome ORPHA:238517
    - Hypoxanthine-guanine phosphoribosyltransferase deficiency ORPHA:206428
    - Idiopathic hypercalciuria ORPHA:2197
    - Infantile nephropathic cystinosis ORPHA:411629
    - Jeune syndrome ORPHA:474
    - Joubert syndrome with oculorenal defect ORPHA:2318
    - Joubert syndrome with renal defect ORPHA:220497
    - Juvenile nephropathic cystinosis ORPHA:411634
    - Karyomegalic interstitial nephritis ORPHA:401996
    - LCAT deficiency ORPHA:650
    - Liddle syndrome ORPHA:526
    - Mitochondrial DNA depletion syndrome, hepatocerebrorenal form ORPHA:363534
    - Multiloculated renal cyst ORPHA:97366
    - Nephroblastoma ORPHA:654
    - Nephronophthisis ORPHA:655
    - Neurofibromatosis type 1 ORPHA:636
    - Non-syndromic renal or urinary tract malformation ORPHA:93546
    - Non-syndromic urogenital tract malformation ORPHA:165704
    - Oculocerebrorenal syndrome of Lowe ORPHA:534
    - Primary Fanconi renotubular syndrome ORPHA:3337
    - Primary hyperoxaluria ORPHA:416
    - Primary hypomagnesemia with hypercalciuria and nephrocalcinosis ORPHA:306516
    - Pseudohypoaldosteronism type 2 ORPHA:757
    - Pseudoxanthoma elasticum ORPHA:758
    - Renal cell carcinoma ORPHA:217071
    - Renal-hepatic-pancreatic dysplasia ORPHA:294415
    - RHYNS syndrome ORPHA:140976
    - Saldino-Mainzer syndrome ORPHA:140969
    - Senior-Boichis syndrome ORPHA:84081
    - Senior-Loken syndrome ORPHA:3156
    - Syndromic renal or urinary tract malformation ORPHA:93547
    - Thrombotic thrombocytopenic purpura ORPHA:54057
    - Tuberous sclerosis complex ORPHA:805
    - Tyrosinemia type 1 ORPHA:882
    - Ventriculomegaly-cystic kidney disease ORPHA:443988
    - Vitamin B12-responsive methylmalonic acidemia ORPHA:28
    - Vitamin B12-unresponsive methylmalonic acidemia ORPHA:27
    - Williams syndrome ORPHA:904
    - XY type gonadal dysgenesis-associated anomalies syndrome ORPHA:1770
    - Zellweger syndrome ORPHA:912

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