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Inherited kidney disorder
MONDO:0100191A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the kidney or urinary system.
Also known as: genetic renal disease, inherited kidney disease, inherited renal disorder, nephrogenetic disorder
317 clinical trials for this condition and its sub-types, 1 tagged with Inherited kidney disorder itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Inherited kidney disorder
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Hereditary nephritis 17 trials · 152 incl. sub-types
7 sub-types
- IgA glomerulonephritis 123 trials
- Alport syndrome 17 trials · 18 incl. sub-types Sub-types →
- Immunoglobulin-mediated membranoproliferative glomerulonephritis 12 trials
- C3 glomerulonephritis 7 trials
- Karyomegalic interstitial nephritis 2 trials
- Balkan nephropathy 1 trial
- Complement factor H deficiency 0 trials Sub-types →
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Familial cystic renal disease 0 trials · 72 incl. sub-types
4 sub-types
- Polycystic kidney disease 13 trials · 65 incl. sub-types Sub-types →
- Autosomal dominant medullary cystic kidney disease with or without hyperuricemia 7 trials Sub-types →
- Adult familial nephronophthisis-spastic quadriparesia syndrome 0 trials
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis 0 trials
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Inherited renal tubular disease 0 trials · 40 incl. sub-types
28 sub-types
- Pseudohypoparathyroidism 8 trials · 9 incl. sub-types Sub-types →
- Cystinuria 7 trials Sub-types →
- Dent disease 5 trials Sub-types →
- Familial primary hypomagnesemia 5 trials Sub-types →
- Nephronophthisis 4 trials Sub-types →
- Oculocerebrorenal syndrome 3 trials
- Jeune syndrome 1 trial · 2 incl. sub-types Sub-types →
- Senior-Loken syndrome 1 trial · 2 incl. sub-types Sub-types →
- Hereditary renal hypouricemia 2 trials Sub-types →
- Nephrogenic diabetes insipidus 1 trial · 2 incl. sub-types Sub-types →
- Pseudohypoaldosteronism type 1 1 trial · 2 incl. sub-types Sub-types →
- EAST syndrome 1 trial
- HELIX syndrome 1 trial
- RHYNS syndrome 1 trial
- Nephrogenic syndrome of inappropriate antidiuresis 1 trial
- Bartter syndrome 0 trials Sub-types →
- Gitelman syndrome 0 trials
- Senior-Boichis syndrome 0 trials Sub-types →
- Autosomal dominant proximal renal tubular acidosis 0 trials
- Autosomal recessive proximal renal tubular acidosis 0 trials
- Cranioectodermal dysplasia 0 trials Sub-types →
- Familial juvenile hyperuricemic nephropathy type 2 0 trials
- Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome 0 trials
- Inherited Fanconi renotubular 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
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Familial nephrotic syndrome 0 trials · 22 incl. sub-types
18 sub-types
- Immunoglobulin-mediated membranoproliferative glomerulonephritis 12 trials
- Idiopathic multidrug-resistant nephrotic syndrome 6 trials
- Nephrotic syndrome 14 3 trials
- Nephrotic syndrome, type 4 1 trial
- LAMB2-related infantile-onset nephrotic syndrome 0 trials Sub-types →
- Congenital nephrotic syndrome, Finnish type 0 trials
- Familial idiopathic steroid-resistant nephrotic syndrome 0 trials Sub-types →
- Nephrotic syndrome 15 0 trials
- Nephrotic syndrome 16 0 trials
- Nephrotic syndrome, IIa 26 0 trials
- Nephrotic syndrome, type 17 0 trials
- Nephrotic syndrome, type 18 0 trials
- Nephrotic syndrome, type 19 0 trials
- Nephrotic syndrome, type 20 0 trials
- Nephrotic syndrome, type 21 0 trials
- Nephrotic syndrome, type 22 0 trials
- Nephrotic syndrome, type 23 0 trials
- Nephrotic syndrome, type 24 0 trials
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Congenital anomaly of kidney and urinary tract 7 trials · 14 incl. sub-types
3 sub-types
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Nephrolithiasis, calcium oxalate 13 trials
2 sub-types
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Neurohypophyseal diabetes insipidus 9 trials
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Hereditary renal cell carcinoma 1 trial · 7 incl. sub-types
7 sub-types
- Hereditary clear cell renal cell carcinoma 4 trials
- PAX6-related ocular dysgenesis 0 trials · 2 incl. sub-types Sub-types →
- Hereditary papillary renal cell carcinoma 2 trials
- Adrenocortical carcinoma, hereditary 0 trials
- Aniridia 2 0 trials
- Aniridia 3 0 trials
- Renal cell carcinoma, Xp11-associated 0 trials
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Inherited focal segmental glomerulosclerosis 1 trial · 4 incl. sub-types
8 sub-types
- HIV-associated nephropathy 2 trials
- Focal segmental glomerulosclerosis 2 1 trial
- Focal segmental glomerulosclerosis 1 0 trials
- Focal segmental glomerulosclerosis 5 0 trials
- Focal segmental glomerulosclerosis 6 0 trials
- Focal segmental glomerulosclerosis 7 0 trials
- Focal segmental glomerulosclerosis 8 0 trials
- Focal segmental glomerulosclerosis 9 0 trials
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Inherited pseudohypoaldosteronism 0 trials · 4 incl. sub-types
2 sub-types
- Pseudohypoaldosteronism type 1 1 trial · 2 incl. sub-types Sub-types →
- Pseudohypoaldosteronism type 2 2 trials Sub-types →
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Renal agenesis 1 trial · 2 incl. sub-types
6 sub-types
- Bilateral renal agenesis 2 trials Sub-types →
- Renal agenesis, unilateral 0 trials
- Renal hypodysplasia/aplasia 1 0 trials
- Renal hypodysplasia/aplasia 2 0 trials
- Renal hypodysplasia/aplasia 3 0 trials
- Renal hypodysplasia/aplasia 4 0 trials
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Liddle syndrome 1 trial
3 sub-types
- Liddle syndrome 1 0 trials
- Liddle syndrome 2 0 trials
- Liddle syndrome 3 0 trials
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Hereditary kidney oncocytoma 1 trial
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Prune belly syndrome 1 trial
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Alsing syndrome 0 trials
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6 sub-types
- Familial juvenile hyperuricemic nephropathy type 1 0 trials
- Familial juvenile hyperuricemic nephropathy type 2 0 trials
- Hyperuricemic nephropathy, familial juvenile type 3 0 trials
- Hyperuricemic nephropathy, familial juvenile type 4 0 trials
- Tubulointerstitial kidney disease, autosomal dominant 6 0 trials
- Tubulointerstitial kidney disease, autosomal dominant, 2 0 trials
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Familial renal glucosuria 0 trials
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Fibronectin glomerulopathy 0 trials
2 sub-types
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2 sub-types
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Nail-patella-like renal disease 0 trials
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1 sub-type
- Renal tubular dysgenesis - ACE 0 trials
Most studied deeper sub-types
Autosomal dominant polycystic kidney disease
(59)
Pseudohypoparathyroidism type 1A
(7)
Autosomal recessive polycystic kidney disease
(6)
Nephronophthisis 1
(4)
X-linked Alport syndrome
(3)
Autosomal recessive Alport syndrome
(2)
Isolated optic nerve hypoplasia
(2)
Pseudopseudohypoparathyroidism
(2)
Autosomal dominant pseudohypoaldosteronism type 1
(1)
Diabetes insipidus, nephrogenic, X-linked
(1)
Ellis-van Creveld syndrome
(1)
Hypouricemia, renal
(1)
Hypouricemia, renal 1
(1)
Polycystic kidney disease 1
(1)
Renal hypomagnesemia 3
(1)
Senior-Loken syndrome 1
(1)
ALG9-associated autosomal dominant polycystic kidney disease
(0)
Alport syndrome 3b, autosomal recessive
(0)
Asphyxiating thoracic dystrophy 1
(0)
Asphyxiating thoracic dystrophy 2
(0)