Browse

Explore conditions, clinical trials, and the organisations running them.

Up to: Hereditary disease · Kidney disorder

Inherited kidney disorder

A 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.

1 trial tagged with this condition →

Hereditary nephritis 17 trials · 152 incl. sub-types Sub-types →
Familial cystic renal disease 0 trials · 72 incl. sub-types Sub-types →
Inherited renal tubular disease 0 trials · 40 incl. sub-types Sub-types →
Familial nephrotic syndrome 0 trials · 22 incl. sub-types Sub-types →
Congenital anomaly of kidney and urinary tract 7 trials · 14 incl. sub-types Sub-types →
Nephrolithiasis, calcium oxalate 13 trials Sub-types →
Neurohypophyseal diabetes insipidus 9 trials
Hereditary renal cell carcinoma 1 trial · 7 incl. sub-types Sub-types →
Inherited focal segmental glomerulosclerosis 1 trial · 4 incl. sub-types Sub-types →
Inherited pseudohypoaldosteronism 0 trials · 4 incl. sub-types Sub-types →
Renal agenesis 1 trial · 2 incl. sub-types Sub-types →
Liddle syndrome 1 trial Sub-types →
Hereditary kidney oncocytoma 1 trial
Prune belly syndrome 1 trial
Alsing syndrome 0 trials
Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation 0 trials
Familial juvenile hyperuricemic nephropathy 0 trials Sub-types →
Familial renal glucosuria 0 trials
Fibronectin glomerulopathy 0 trials Sub-types →
Hypophosphatemic nephrolithiasis/osteoporosis 1 0 trials
Hypophosphatemic nephrolithiasis/osteoporosis 2 0 trials
Inherited distal renal tubular acidosis 0 trials Sub-types →
Nail-patella-like renal disease 0 trials
Nephrolithiasis, X-linked recessive, with renal failure 0 trials
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis 0 trials
Renal tubular dysgenesis of genetic origin 0 trials Sub-types →