Directory
Familial hypertension
Hypertension, also known as arterial hypertension, is a condition characterized by elevated blood pressure (BP)...
Familial hypertriglyceridemia
Familial hypertriglyceridemia is an inherited disorder characterized by elevated levels of triglycerides in the blood,...
Familial hypertrophic cardiomyopathy
Familial hypertrophic cardiomyopathy (FHCM) is a genetic disorder characterized by thickening of the...
Familial hypercholesterolemia
Familial hypercholesterolemia (FH) is an inherited disorder characterized by high levels of cholesterol in the blood...
Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia is a rare inherited disorder characterized by low levels of lipoproteins...
Familial hypocalciuric hypercalcemia type 1
Familial hypocalciuric hypercalcemia (FHCH) is a genetic disorder characterized by elevated calcium levels in the blood...
Familial hypofibrinogenemia
Familial hypofibrinogenemia is an inherited coagulopathic condition characterized by significantly reduced levels of fibr...
Familial deafness
Familial deafness, or hereditary hearing loss, is a group of disorders characterized by hearing loss that is transmitted through...
Familial dilated cardiomyopathy
Familial dilated cardiomyopathy (DCM) is a disease characterized by dilation of the heart chambers and its structure...
Familial Dysautonomia
Familial dysautonomia, also known as familial autonomic syndrome, is a rare inherited disorder associated with...
Familial ventricular tachycardia
Familial ventricular tachycardia (FVT) is an inherited disorder characterized by recurring episodes of...
Familial combined hyperlipidemia
Familial combined hyperlipidemia is an inherited disorder characterized by elevated levels of lipids in the pla...
Familial Short Stature (FSS)
Familial short stature (FSS) is a genetic disorder characterized by short stature within a family, with parameters...
Familial Wilms tumor 2
Familial Wilms tumor (FWT) is a rare type of kidney tumor that most commonly occurs in childhood. It occurs in...
Familial paroxysmal nonkinesigenic dyskinesia
Familial paroxysmal nonkinesigenic dyskinesia (FPND) is a rare neurological disorder characterized by increased...
Familial partial lipodystrophy
Familial partial lipodystrophy (FPLD) is a rare genetic disorder characterized by symmetrical loss of fat...
Familial porencephaly
Familial porencephaly is a rare inherited disorder characterized by abnormal development of the brain, which in most cases...
Familial mixed cryoglobulinemia
Familial mixed cryoglobulinemia is a rare disorder characterized by the presence of cryoglobulins in the blood serum,...
Familial Mediterranean fever
Familial Mediterranean fever (FMF) is a genetically determined disease that belongs to a group of hereditary hemorrhagic...
Familial exudative vitreoretinopathy
Familial exudative vitreoretinopathy (FEVR) is a hereditary disease characterized by pathological changes in the...
Familial adenomatous polyposis
Familial adenomatous polyposis (FAP) is a hereditary disease characterized by the formation of numerous adenomatous polyps ...
Familial hyperaldosteronism
Familial hyperaldosteronism (FH) is a hereditary disorder that involves excess production of aldosterone, ...
Familial hyperthyroidism caused by mutations in the TSH receptor
Familial hyperthyroidism caused by mutations in the TSH receptor is a rare inherited disorder characterized by excess...
Familial hypopituitarism
Familial hypopituitarism is a rare genetic disorder characterized by deficiencies of several hormones, which are...
Familial HDL deficiency
Familial HDL (high-density lipoprotein) deficiency is a rare inherited disorder characterized by severe...
Familial glucocorticoid deficiency
Familial glucocorticoid deficiency (FGCD) is a rare inherited disorder characterized by insufficient production of...
Familial lipoprotein lipase deficiency
Familial lipoprotein lipase deficiency (FLLD) is a rare genetic disorder characterized by insufficient activity of...
Familial benign copper deficiency
Familial benign copper deficiency, also known as cystic fibrosis copper or Wilson's disease, is a genetic disorder that causes...
Familial isolated hyperparathyroidism
Familial isolated hyperparathyroidism (SIHP) is a rare inherited disorder characterized by excess production of para...
Familial colorectal cancer
Familial colorectal cancer is a group of genetically determined diseases characterized by the development of malignant...
