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'...

Agammaglobulinemia 8b, autosomal recessive is a rare genetic condition. Information about the overall characteristics of this condition is currently l...

Agammaglobulinemia 9, autosomal recessive is a primary immunodeficiency that affects how the immune system fights infections. People with this conditi...

Agammaglobulinemia, autosomal recessive, due to BOB1 deficiency is a condition where the immune system is affected by low levels of antibodies, caused...

This syndrome is a rare condition seen in a small number of siblings. People with this condition have agammaglobulinemia, which means they have very l...

AGAT deficiency is a very rare metabolic disorder that primarily affects creatine synthesis, leading to global developmental delay, intellectual disab...

Agenesis and aplasia of the uterine body is a rare condition where the main part of the uterus is either absent (agenesis) or underdeveloped (aplasia)...

This condition is a neurodegenerative disorder marked by severe, progressive sensorimotor neuropathy that begins in infancy. It affects the nerves tha...

Agenesis of the superior vena cava is a rare congenital condition in which one or both of the major veins that carry blood from the upper body to the...

Age-related clonal hematopoiesis (ARCH) is a precancerous condition. It is marked by a slow, clonal expansion of blood stem cells that have acquired s...

Age related macular degeneration 1 is an eye condition that affects the macula, the part of the retina responsible for clear and detailed central visi...

Information about overview is currently limited for this condition.

Age related macular degeneration 11 is a form of age-related macular degeneration that is caused by a mutation in the CST3 gene. This condition is kno...

Age related macular degeneration 12 is a form of age-related macular degeneration that happens because of a mutation in the CX3CR1 gene. Macular degen...

Age related macular degeneration 14 is a condition linked to changes near the C2 and CFB genes on chromosome 6p21. These genetic variations may influe...

Age related macular degeneration 2 is a condition that affects the central part of the retina, known as the macula. This condition is linked to variat...