Disease Directory

Adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia, also known as NI-PHH, is a form of congenital isolated hyperinsulinism. This cond...

Adult-onset progressive leukoencephalopathy-early-onset deafness is a rare genetic neurological disorder. It is characterized by congenital or early-o...

Adult-onset proximal spinal muscular atrophy, autosomal dominant is a rare neuromuscular condition. It is also known by several other names such as Fi...

adult-onset segmental dystonia is a rare disease. Detailed information about this condition is currently limited in medical literature.

Advance sleep phase syndrome, familial, 4 is a rare inherited condition that affects the timing of sleep. People with this condition may experience a...

Advanced sleep phase syndrome is a very rare circadian rhythm sleep disorder. It is characterized by a very early sleep onset and an early waking time...

Advanced sleep phase syndrome 1 is a rare condition that affects how a person's sleep-wake cycle is regulated. It is characterized by an earlier onset...

Advanced sleep phase syndrome 2 is a condition that affects the body’s natural sleep-wake cycle. This condition is defined as any advanced sleep phase...

Advanced sleep phase syndrome 3 is a condition characterized by a shift in the timing of a person's sleep and wake patterns. People with this conditio...

Aerobic Actinomyces infection is a condition caused by an infection with a less common type of Actinomyces bacteria that require oxygen for growth. Th...

Aflatoxin-related hepatocellular carcinoma is a type of liver cancer that develops following exposure to aflatoxin, a potent carcinogen produced by ce...

Agammaglobulinemia is a condition where there is a decreased level of immunoglobulins in the blood. Immunoglobulins are proteins important for fightin...

Agammaglobulinemia 10, autosomal dominant is a condition that usually begins in early childhood. People with this condition experience recurrent viral...

Agammaglobulinemia 2, autosomal recessive is a rare condition that falls under the group of autosomal agammaglobulinemias. The disease is caused by a...

Agammaglobulinemia 3, autosomal recessive is a rare condition caused by a mutation in the CD79A gene. This disease affects the body’s ability to produ...

Agammaglobulinemia 4, autosomal recessive is a rare condition in which there is a problem with the immune system. The condition is due to a mutation i...

Agammaglobulinemia 5, autosomal dominant is a rare immune condition in which a mutation in the LRRC8A gene leads to difficulties in producing antibodi...

Agammaglobulinemia 6, autosomal recessive is a rare genetic condition where mutations in the CD79B gene affect the immune system. This condition falls...

Agammaglobulinemia 7, autosomal recessive is a rare condition caused by a mutation in the PIK3R1 gene. This mutation affects the immune system by disr...

Agammaglobulinemia 8, autosomal dominant is a rare condition that affects the body's immune system. It is defined by a problem with the immune system'...