Primary aldosteronism (al-DOS-tuh-ro-niz-um) is a type of hormonal disorder that leads to high blood pressure. Your adrenal glands produce a number of essential hormones. One of these is aldosterone, which balances sodium and potassium in your blo...

ALECT2 amyloidosis is a rare, inherited form of amyloidosis caused by a mutation in the ALECT2 gene. It is characterized by the buildup of abnormal proteins in the body's organs and tissues, leading to organ damage and other health problems. Sympt...

Alexander disease is named after the physician who first described the condition in 1949 (WS Alexander). It is an extremely rare, usually progressive and fatal, neurological disorder. Initially it was detected most often during infancy or early ch...

Alexander Disease is a rare neurological disorder that affects the brain and spinal cord. It is caused by a mutation in the GFAP gene, which is responsible for producing the protein glial fibrillary acidic protein (GFAP). This protein is essential...

Alexander disease type I is a rare, fatal neurological disorder that affects the central nervous system. It is caused by a mutation in the GFAP gene, which is responsible for producing the protein glial fibrillary acidic protein (GFAP). This prote...

Alexander disease type II is a rare, progressive neurological disorder caused by mutations in the GFAP gene. It is characterized by the accumulation of abnormal proteins in the brain, which can lead to seizures, developmental delays, and progressi...

ALG1-CDG is an algorithm for computing the minimum cost of a directed graph. It is based on the Bellman-Ford algorithm and is used to find the shortest path between two nodes in a graph....

ALG11-CDG is a gene mutation that is associated with a rare form of inherited intellectual disability. It is caused by a mutation in the ALG11 gene, which is located on chromosome 11. The mutation results in a decrease in the activity of the ALG11...

ALG12-CDG is a flight route operated by Air Algerie, connecting Algiers, Algeria to Charles de Gaulle Airport in Paris, France....

ALG13-CDG is a gene mutation that is associated with a rare form of inherited epilepsy known as Autosomal Recessive Primary Microcephaly (ARPM). This mutation is caused by a change in the ALG13 gene, which is responsible for the production of an e...

ALG2-CDG is an abbreviation for the German language course "Algebra 2 - Computational Discrete Geometry". It is a course designed to teach students the fundamentals of algebra and discrete geometry, as well as how to use computers to solve problem...

ALG3-CDG is a gene mutation that is associated with a rare form of congenital disorder of glycosylation (CDG). It is caused by a mutation in the ALG3 gene, which is responsible for the production of an enzyme involved in the synthesis of N-linked ...

ALG6-CDG is a gene mutation that is associated with a rare form of congenital muscular dystrophy. It is caused by a mutation in the ALG6 gene, which is located on chromosome 9. The mutation results in a deficiency of the enzyme alglucosidase 6, wh...

ALG8-CDG is a gene mutation that is associated with a rare form of congenital disorder of glycosylation (CDG). It is caused by a mutation in the ALG8 gene, which is responsible for the production of an enzyme involved in the synthesis of glycoprot...

ALG9-CDG is a flight route operated by Air Algerie, connecting Algiers, Algeria to Charles de Gaulle Airport in Paris, France....

Reflex sympathetic dystrophy syndrome (RSDS), also known as complex regional pain syndrome, is a rare disorder of the sympathetic nervous system that is characterized by chronic, severe pain. The sympathetic nervous system is that part of the auto...

Reflex sympathetic dystrophy syndrome (RSDS), also known as complex regional pain syndrome, is a rare disorder of the sympathetic nervous system that is characterized by chronic, severe pain. The sympathetic nervous system is that part of the auto...