Alopecia, isolated is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Alopecia mucinosa is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Alopecia universalis is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Alopecia universalis onychodystrophy vitiligo is an extremely rare condition. Because few cases have been documented, detailed clinical information is...

Alpha 1-antitrypsin deficiency is a hereditary condition that primarily affects the liver and lungs, often manifesting in adulthood. It is caused by c...

Alpha-2-plasmin inhibitor deficiency is a rare inherited bleeding disorder caused by a shortage of the alpha2 antiplasmin protein, which normally help...

alpha-actinopathy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

alpha granule disease is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Alpha-heavy chain disease is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Alpha-mannosidosis is an inherited lysosomal storage disorder that primarily affects multiple organ systems, including the immune system, skeletal str...

Alpha-mannosidosis is a rare lysosomal storage disorder caused by a deficiency in the enzyme alpha-D-mannosidase. The adult form of this condition is...

Alpha-mannosidosis, infantile form, is a rare lysosomal storage disorder characterized by a deficiency in the enzyme alpha-D-mannosidase. Currently, n...

alpha-mannosidosis type 1 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Alpha-methylacyl-CoA racemase deficiency is an inherited metabolic disorder that chiefly affects the nervous system and eyes. It results from harmful...

alpha-N-acetylgalactosaminidase deficiency is an extremely rare condition. Because few cases have been documented, detailed clinical information is li...

Alpha-N-acetylgalactosaminidase deficiency type 1 is a very rare disorder that primarily affects the central nervous system, manifesting as infantile...

Alpha-N-acetylgalactosaminidase deficiency type 2 is a very rare adult-onset condition caused by changes in the NAGA gene. It is part of a group of di...

alpha-N-acetylgalactosaminidase deficiency type 3 is an extremely rare condition. Because few cases have been documented, detailed clinical informatio...

Alpha thalassemia-intellectual disability syndrome type 1 (ATR-16) is a very rare contiguous gene deletion syndrome that affects blood formation and n...

Alpha-thalassemia-myelodysplastic syndrome (ATMDS) is an acquired disorder characterized by abnormal red blood cell production related to a myelodyspl...