Disease Directory

Familial ovarian cancer is a form of ovarian cancer that happens because of an inherited change in the genome. This means that the alteration in the g...

Familial ovarian carcinoma refers to ovarian cancer that appears in relatives of individuals with a history of the disease. This condition affects the...

Familial pancreatic carcinoma is a form of pancreatic cancer that occurs in families with two or more first‐degree relatives affected by the disease....

Familial papillary or follicular thyroid carcinoma is a form of thyroid cancer that occurs within families and is distinguished by tumors that are oft...

Familial papillary thyroid carcinoma with renal papillary neoplasia is an extremely rare inherited tumor syndrome that falls within the familial nonme...

Familial partial epilepsy is an inherited form of epilepsy that primarily affects the electrical activity in specific regions of the brain. This condi...

Familial partial lipodystrophy is a group of rare genetic syndromes characterized by an abnormal loss of fat from the limbs and buttocks, often presen...

Familial partial lipodystrophy, Dunnigan type is a rare inherited disorder that affects the distribution of body fat and is characterized by loss of s...

Familial partial lipodystrophy, Kobberling type is a very rare condition characterized by an abnormal distribution of body fat, where fat is reduced i...

Familial periodic paralysis refers to a group of genetic neurological disorders marked by sudden, temporary episodes of muscle weakness or paralysis....

Familial polycythemia is a condition characterized by an increased production of red blood cells that tends to occur in families. Research has identif...

Familial primary hyperparathyroidism is an inherited form of primary hyperparathyroidism that results from genetic alterations affecting the parathyro...

Familial primary hypomagnesemia is a hereditary condition characterized by a selective defect in renal or intestinal magnesium absorption that leads t...

Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), also known as Michellis-Castrillo syndrome, is a kidney disorder cha...

Familial primary hypomagnesemia with hypocalcuria is a condition that affects the body’s electrolyte balance, primarily involving the regulation of ma...

Familial primary hypomagnesemia with normocalcuria is a condition characterized by abnormally low magnesium levels in the blood while calcium levels r...