Inherited renal tubular disease

Part of

Sub-types of Inherited renal tubular disease

• Pseudohypoparathyroidism 8 trials · 9 incl. sub-types
  5 sub-types

  • Pseudohypoparathyroidism type 1A 7 trials
  • Pseudopseudohypoparathyroidism 2 trials
  • Pseudohypoparathyroidism type 1B 0 trials
  • Pseudohypoparathyroidism type 1C 0 trials
  • Pseudohypoparathyroidism type 2 0 trials
• Cystinuria 7 trials
  2 sub-types

  • Cystinuria type A 0 trials
  • Cystinuria type B 0 trials
• Dent disease 5 trials
  2 sub-types

  • Dent disease type 1 0 trials
  • Dent disease type 2 0 trials
• Familial primary hypomagnesemia 5 trials
  5 sub-types

  • Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis 0 trials · 1 incl. sub-types Sub-types →
  • EGF-related primary hypomagnesemia with intellectual disability 0 trials
  • Familial primary hypomagnesemia with hypocalcuria 0 trials Sub-types →
  • Familial primary hypomagnesemia with normocalcuria 0 trials Sub-types →
  • Hypomagnesemia 7, renal, with or without dilated cardiomyopathy 0 trials
• Nephronophthisis 4 trials
  18 sub-types

  • Nephronophthisis 1 4 trials
  • Late-onset nephronophthisis 0 trials
  • Nephronophthisis 11 0 trials
  • Nephronophthisis 12 0 trials
  • Nephronophthisis 13 0 trials
  • Nephronophthisis 14 0 trials
  • Nephronophthisis 15 0 trials
  • Nephronophthisis 16 0 trials
  • Nephronophthisis 18 0 trials
  • Nephronophthisis 19 0 trials
  • Nephronophthisis 2 0 trials
  • Nephronophthisis 20 0 trials
  • Nephronophthisis 3 0 trials
  • Nephronophthisis 4 0 trials
  • Nephronophthisis 7 0 trials
  • Nephronophthisis 9 0 trials
  • Nephronophthisis-like nephropathy 1 0 trials
  • Nephronophthisis-like nephropathy 2 0 trials
• Oculocerebrorenal syndrome 3 trials
• Hereditary renal hypouricemia 2 trials
  3 sub-types

  • Hypouricemia, renal 1 trial · 2 incl. sub-types Sub-types →
  • Hypouricemia, familial renal, due to tubular hypersecretion 0 trials
  • Hypouricemia, hypercalcinuria, and decreased bone density 0 trials
• Jeune syndrome 1 trial · 2 incl. sub-types
  24 sub-types

  • Ellis-van Creveld syndrome 1 trial Sub-types →
  • Beemer-Langer syndrome 0 trials
  • Jeune syndrome - GRK2-related 0 trials
  • Asphyxiating thoracic dystrophy 1 0 trials
  • Asphyxiating thoracic dystrophy 2 0 trials
  • Asphyxiating thoracic dystrophy 3 0 trials
  • Asphyxiating thoracic dystrophy 4 0 trials
  • Asphyxiating thoracic dystrophy 5 0 trials
  • Short-rib thoracic dysplasia 10 with or without polydactyly 0 trials
  • Short-rib thoracic dysplasia 11 with or without polydactyly 0 trials
  • Short-rib thoracic dysplasia 13 with or without polydactyly 0 trials
  • Short-rib thoracic dysplasia 14 with polydactyly 0 trials
  • Short-rib thoracic dysplasia 15 with polydactyly 0 trials
  • Short-rib thoracic dysplasia 16 with or without polydactyly 0 trials
  • Short-rib thoracic dysplasia 17 with or without polydactyly 0 trials
  • Short-rib thoracic dysplasia 18 with polydactyly 0 trials
  • Short-rib thoracic dysplasia 19 with or without polydactyly 0 trials
  • Short-rib thoracic dysplasia 20 with polydactyly 0 trials
  • Short-rib thoracic dysplasia 21 without polydactyly 0 trials
  • Short-rib thoracic dysplasia 22 without polydactyly 0 trials
  • Short-rib thoracic dysplasia 6 with or without polydactyly 0 trials
  • Short-rib thoracic dysplasia 7 with or without polydactyly 0 trials
  • Short-rib thoracic dysplasia 8 with or without polydactyly 0 trials
  • Short-rib thoracic dysplasia 9 with or without polydactyly 0 trials
• Senior-Loken syndrome 1 trial · 2 incl. sub-types
  9 sub-types

  • Senior-Loken syndrome 1 1 trial
  • Senior-Loken syndrome 4 0 trials
  • Senior-Loken syndrome 5 0 trials
  • Senior-Loken syndrome 6 0 trials
  • Senior-Loken syndrome 7 0 trials
  • Senior-Loken syndrome 8 0 trials
  • Senior-Loken syndrome 9 0 trials
  • Nephronophthisis 15 0 trials
  • Senior-loken syndrome 3 0 trials
• Nephrogenic diabetes insipidus 1 trial · 2 incl. sub-types
  2 sub-types

  • Diabetes insipidus, nephrogenic, X-linked 1 trial
  • Diabetes insipidus, nephrogenic, autosomal 0 trials
• Pseudohypoaldosteronism type 1 1 trial · 2 incl. sub-types
  4 sub-types

  • Autosomal dominant pseudohypoaldosteronism type 1 1 trial
  • Pseudohypoaldosteronism, type IB1, autosomal recessive 0 trials
  • Pseudohypoaldosteronism, type IB2, autosomal recessive 0 trials
  • Pseudohypoaldosteronism, type IB3, autosomal recessive 0 trials
• EAST syndrome 1 trial
• HELIX syndrome 1 trial
• RHYNS syndrome 1 trial
• Nephrogenic syndrome of inappropriate antidiuresis 1 trial
• Bartter syndrome 0 trials
  6 sub-types

  • Bartter disease type 1 0 trials
  • Bartter disease type 2 0 trials
  • Bartter disease type 3 0 trials
  • Bartter disease type 5 0 trials
  • Bartter syndrome type 4 0 trials Sub-types →
  • Bartter syndrome with hypocalcemia 0 trials
• Gitelman syndrome 0 trials
• Senior-Boichis syndrome 0 trials
  1 sub-type

  • Nephronophthisis 11 0 trials
• Autosomal dominant proximal renal tubular acidosis 0 trials
• Autosomal recessive proximal renal tubular acidosis 0 trials
• Cranioectodermal dysplasia 0 trials
  7 sub-types

  • Cranioectodermal dysplasia 1 0 trials
  • Cranioectodermal dysplasia 2 0 trials
  • Cranioectodermal dysplasia 3 0 trials
  • Cranioectodermal dysplasia 4 0 trials
  • Cranioectodermal dysplasia 5 0 trials
  • Cranioectodermal dysplasia 6 0 trials
  • Short-rib thoracic dysplasia 16 with or without polydactyly 0 trials
• Familial juvenile hyperuricemic nephropathy type 2 0 trials
• Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome 0 trials
• Inherited Fanconi renotubular syndrome 0 trials
  3 sub-types

  • Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young 0 trials
  • Fanconi renotubular syndrome 5 0 trials
  • Primary Fanconi syndrome 0 trials Sub-types →
• Mitochondrial DNA depletion syndrome, hepatocerebrorenal form 0 trials
• Nephrogenic diabetes insipidus-intracranial calcification syndrome 0 trials
• Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome 0 trials
• Renal tubular acidosis, distal, 3, with or without sensorineural hearing loss 0 trials