Renal tubular transport disease

MONDO:0006510

Genetic defects in the selective or non-selective transport functions of the kidney tubules.

Also known as: disorder of renal absorption, renal absorption disease, kidney tubular transport, inborn error, kidney tubular transport, inborn errors, renal tubular transport errors, renal tubular transport, inborn error

17 clinical trials for this condition and its sub-types, 0 tagged with Renal tubular transport disease itself.

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Where it sits in the disease tree

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Part of

↑ Kidney disorder (4032)

Sub-types of Renal tubular transport disease

Dent disease 5 trials
2 sub-types
- Dent disease type 1 0 trials
- Dent disease type 2 0 trials
Pseudohypoaldosteronism 3 trials · 5 incl. sub-types
2 sub-types
- Inherited pseudohypoaldosteronism 0 trials · 4 incl. sub-types Sub-types →
- Transient pseudohypoaldosteronism 0 trials
Fanconi renotubular syndrome 4 trials
4 sub-types
- Deal Barratt Dillon syndrome 0 trials
- Acquired Fanconi syndrome 0 trials Sub-types →
- Adult Fanconi syndrome 0 trials
- Inherited Fanconi renotubular syndrome 0 trials Sub-types →
Renal tubular acidosis 2 trials
5 sub-types
- Hyperkalemic renal tubular acidosis 0 trials
- Neuroaxonal dystrophy renal tubular acidosis 0 trials
- Proximal renal tubular acidosis 0 trials Sub-types →
- Renal tubular acidosis 3 0 trials
- Renal tubular acidosis, distal, 3, with or without sensorineural hearing loss 0 trials
Liddle syndrome 1 trial
3 sub-types
- Liddle syndrome 1 0 trials
- Liddle syndrome 2 0 trials
- Liddle syndrome 3 0 trials
Renal hypomagnesemia 3 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
Familial renal glucosuria 0 trials

Most studied deeper sub-types

Pseudohypoaldosteronism type 2 (2) Autosomal dominant pseudohypoaldosteronism type 1 (1) Pseudohypoaldosteronism type 1 (1) Autosomal dominant proximal renal tubular acidosis (0) Autosomal recessive proximal renal tubular acidosis (0) Bartter disease type 4A (0) Bartter disease type 4B (0) Fanconi renotubular syndrome 1 (0) Fanconi renotubular syndrome 2 (0) Fanconi renotubular syndrome 3 (0) Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young (0) Fanconi renotubular syndrome 5 (0) Preeyasombat-Varavithya syndrome (0) Primary Fanconi syndrome (0) Pseudohypoaldosteronism type 2A (0) Pseudohypoaldosteronism type 2B (0) Pseudohypoaldosteronism type 2C (0) Pseudohypoaldosteronism type 2D (0) Pseudohypoaldosteronism type 2E (0) Pseudohypoaldosteronism, type IB1, autosomal recessive (0)

Including sub-types (17) Tagged with Renal tubular transport disease (0)

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