Kidney and Urinary Diseases | Page 2

292 diseases found in 3 pages

F Diseases

Familial LCAT deficiency Familial Mediterranean fever Familial prostate cancer Fanconi anemia Fanconi Bickel syndrome Fanconi syndrome Feigenbaum Bergeron Richardson syndrome Fibrillary glomerulonephritis Fibromuscular dysplasia Fish-eye disease Fitzsimmons Walson Mellor syndrome Focal segmental glomerulosclerosis Fowler's syndrome Fraser syndrome Frasier syndrome

G Diseases

Galactokinase deficiency Galloway-Mowat syndrome Genito palato cardiac syndrome Giant cell arteritis Gitelman syndrome Glomerulonephritis Glomerulopathy with fibronectin deposits 1 Glomerulopathy with fibronectin deposits 2 Glucocorticoid-remediable aldosteronism Glycogen storage disease type 1A Glycogen storage disease type 1B Goodpasture syndrome Graham Boyle Troxell syndrome Granulomatosis with polyangiitis

H Diseases

Hartnup disease Henoch-Schonlein purpura Hepatoerythropoietic porphyria Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome Hereditary coproporphyria Hereditary endotheliopathy, retinopathy, nephropathy, and stroke Hereditary fructose intolerance Hereditary leiomyomatosis and renal cell cancer Hereditary paraganglioma-pheochromocytoma Hyperparathyroidism-jaw tumor syndrome Hypocomplementemic urticarial vasculitis Hypophosphatemic rickets Hypospadias familial Hypospadias-intellectual disability, Goldblatt type syndrome Hypotelorism cleft palate hypospadias Hypotrichosis-lymphedema-telangiectasia syndrome

I Diseases

Ichthyosis, mental retardation, dwarfism and renal impairment IgA nephropathy IMAGe syndrome Imerslund-Grasbeck syndrome Immunotactoid glomerulopathy Infundibulopelvic dysgenesis Interstitial cystitis Ivemark syndrome

J Diseases

Jeune syndrome Joubert syndrome with oculorenal anomalies Juberg Marsidi syndrome Juvenile dermatomyositis Juvenile polymyositis

K Diseases

Kawasaki disease

L Diseases

Lesch Nyhan syndrome Liddle syndrome Limited cutaneous systemic sclerosis Limited systemic sclerosis Lowe oculocerebrorenal syndrome Lupus nephritis

M Diseases

Male pseudohermaphroditism intellectual disability syndrome, Verloes type Maturity-onset diabetes of the young, type 5 Meacham Winn Culler syndrome Meckel syndrome Megacystis microcolon intestinal hypoperistalsis syndrome Membranous nephropathy Methylcobalamin deficiency cbl G type Methylmalonic acidemia Methylmalonic aciduria, cblA type Methylmalonic aciduria, cblB type Microscopic polyangiitis Minimal change disease Mixed connective tissue disease Muckle-Wells syndrome Multicentric carpotarsal osteolysis syndrome Multicystic renal dysplasia, bilateral Multisystemic smooth muscle dysfunction syndrome MURCS association Musculocontractural Ehlers-Danlos syndrome

N Diseases

Naguib-Richieri-Costa syndrome Nail-patella syndrome Nephrocalcinosis Nephrogenic diabetes insipidus Nephronophthisis Neurofaciodigitorenal syndrome Noonan syndrome Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6

O Diseases

Ochoa syndrome Oculo skeletal renal syndrome Oligomeganephronic renal hypoplasia

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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