Familial renal disease is an uncommon cause of kidney failure in dogs and cats. Most causes are breed-related (familial) and some are inherited. Some...

with Fanconi anemia, a separate disease.[citation needed] Familial renal disease in animals for Fanconi syndrome in Basenjis "Fanconi syndrome" at Dorland's...

stone disease, also known as renal calculus disease, nephrolithiasis or urolithiasis, is a crystallopathy where a solid piece of material (renal calculus)...

Optic disc drusen Optic nerve coloboma with renal disease Optic nerve disorder Optic nerve hypoplasia, familial bilateral Optic neuritis Optic pathway glioma...

developing of certain diseases such as renal microvascular disease and capillary rarefaction may relate to this decrease in efficiency of sodium excretion. There...

the disease range from 14 to 34%. Rarely, it is associated with clear cell renal cell carcinoma and papillary renal cell carcinoma. If it develops in someone...

aldosterone-producing cells of the adrenal cortex resulting in primary hyperaldosteronism. Two familial forms have been identified: type I (dexamethasone suppressible)...

hypercoagulability. Familial renal disease is an uncommon cause of kidney failure in young dogs. Most causes are breed-related (familial) and some are inherited...

adenitis". Companion Animal. 11 (5): 62–8. doi:10.1111/j.2044-3862.2006.tb00066.x. Bernard, MA; Valli, VE (1977). "Familial renal disease in Samoyed dogs"....

renal in nature, including proteinuria, nephrotic syndrome and progressive development of chronic kidney disease leading to end stage kidney disease (ESKD)...

these diseases are mainly sporadic and only a few cases are familial. Others are only familial. Some result from medical treatment. Prions are an infectious...

including: allergic skin disease, cutaneous mucinosis, intertrigo, otitis externa, and vasculopathy. Shar Pei fever (also called familial Shar Pei fever or FSF)...

causes retinitis pigmentosa, which also affects humans. Familial renal disease is inherited in Abyssinians and Persians Feline hypertrophic cardiomyopathy...

Persian-related breeds. In the same study, all six Maine Coon cats with renal cysts tested negative for the PKD1 mutation, proving the disease in these cats to...

syndrome) Familial benign chronic pemphigus (familial benign pemphigus, Hailey–Hailey disease) Fanconi syndrome (familial pancytopenia, familial panmyelophthisis)...

Pion PD, et al. (June 1999). "Familial hypertrophic cardiomyopathy in maine coon cats: an animal model of human disease". Circulation. 99 (24): 3172–3180...

Coronavirus disease 2019 (COVID-19) is a contagious disease caused by the coronavirus SARS-CoV-2. The first known case was identified in Wuhan, China, in December...

often involves SLE-induced neurologic disease, renal failure, and/or the macrophage activation syndrome. Mutations in about 40 genes have been reported to...

problems causing renal artery hypotension, with the result that CO remains chronically elevated.[citation needed] This includes diseases such as polycystic...

cerebral circulation to the brain, renal circulation to the kidneys, and bronchial circulation to the bronchi in the lungs. The human circulatory system...

TGF-beta1 are protected against renal fibrosis in obstructive kidney disease". American Journal of Physiology. Renal Physiology. 295 (1): F118–27. doi:10...

eyes, and tremor. Renal artery stenosis may be associated with a localized abdominal bruit to the left or right of the midline, or in both locations. Coarctation...

secretion. The rare genetic disorders familial juvenile hyperuricemic nephropathy, medullary cystic kidney disease, phosphoribosylpyrophosphate synthetase...

renal arteries, which supply blood to the kidneys. Plaque occurrence and accumulation lead to decreased kidney blood flow and chronic kidney disease,...

Familial adenomatous polyposis (FAP) is an autosomal dominant inherited condition in which numerous adenomatous polyps form mainly in the epithelium of...

behaviour. Familial renal amyloidosis or AA amyloidosis, a kidney disorder due to a mutation in the AA amyloid protein gene, has been seen in Abyssinians...

disorders, whether or not renal calcification is involved. The most studied disease is Dent's disease, which is attributed to a mutation in CLCN5 or OCRL1 genes...

no symptoms are noticed initially. As it progresses, bone pain, anemia, renal insufficiency, and infections may occur. Complications may include hypercalcemia...

Coronary artery disease (CAD), also called coronary heart disease (CHD), or ischemic heart disease (IHD), is a type of heart disease involving the reduction...

many pediatric liver diseases, including biliary atresia, alpha-1 antitrypsin deficiency, alagille syndrome, progressive familial intrahepatic cholestasis...