Inherited orthostatic hypotension is a condition in which individuals experience a significant drop in blood pressure upon standing, leading to sympto...

Inherited porphyria refers to a group of eight hereditary metabolic disorders that affect porphyrin and heme metabolism. The condition is characterize...

Inherited primary ovarian failure is a condition affecting the ovaries, where ovarian function declines prematurely due to changes in the individual’s...

Inherited pseudohypoaldosteronism is a condition in which the body exhibits a decreased responsiveness to aldosterone, a hormone important for maintai...

Inherited pseudoxanthoma elasticum is a condition in which calcium and other minerals accumulate in the elastic fibers of the skin, eyes, and blood ve...

Inherited reflex epilepsy, also known as hereditary reflex epilepsy, is a form of epilepsy in which seizures are triggered by specific stimuli due to...

Inherited renal tubular disease is an umbrella term for a group of disorders that affect the kidney’s ability to properly reabsorb substances, with se...

Inherited retinal dystrophy is a form of retinal degeneration caused by inherited changes in the genome that affect the normal function of the retina....

Inherited rippling muscle disease is a rare neuromuscular disorder that primarily affects skeletal muscle function. The condition is characterized by...

Inherited sideroblastic anemia is a condition characterized by abnormal iron accumulation in the precursors of red blood cells, often resulting in ine...

Inherited thrombocytopenia is a condition characterized by a reduced number of platelets, which are essential for blood clotting. This condition is as...

Inherited thrombophilia is an inherited hypercoagulable disorder that predisposes affected individuals to an increased risk of blood clots. The condit...

Inherited thyroid metabolism disease is an inherited metabolic condition that arises from disruption in the thyroid hormone metabolic process. Althoug...

Inherited torticollis is a congenital benign lesion that affects the distal portion of the sternocleidomastoid muscle in infants. It is characterized...

Inherited vitreoretinopathy is a condition that primarily affects the retina and can lead to vision disturbances. The precise genetic basis is not cur...

Insulin autoimmune syndrome is a very rare condition that leads to episodes of low blood sugar, or hypoglycemia, caused by the body’s immune system mi...

Insulin-resistance syndrome type A is an extreme form of insulin resistance characterized by high levels of insulin, distinctive skin changes known as...