Aniridia Cerebellar Ataxia Mental Deficiency (ACAMD) is a rare genetic disorder characterized by the absence of the iris of the eye (aniridia), ataxia (poor coordination), mental deficiency, and other neurological problems. It is caused by a mutat...

Aniridia-absent patella syndrome is a rare genetic disorder characterized by the absence of the iris of the eye (aniridia), the absence of the kneecap (patella), and other physical abnormalities. It is caused by a mutation in the PAX6 gene, which ...

Aniridia-intellectual disability syndrome is a rare genetic disorder that affects the eyes and the brain. It is characterized by the absence of the iris (the colored part of the eye) and intellectual disability. Other symptoms may include vision p...

Aniridia-ptosis-intellectual disability-familial obesity syndrome is a rare genetic disorder characterized by the presence of aniridia (absence of the iris of the eye), ptosis (drooping of the upper eyelid), intellectual disability, and familial o...

Aniridia-renal agenesis-psychomotor retardation syndrome (ARP) is a rare genetic disorder characterized by the absence of the iris of the eye (aniridia), the absence of one or both kidneys (renal agenesis), and delayed development of physical and ...

Anisakiasis is a parasitic infection caused by eating raw or undercooked fish or seafood that contains larvae of the Anisakis worm. Symptoms of anisakiasis include abdominal pain, nausea, vomiting, and diarrhea. In some cases, the larvae can cause...

Anisocoria is a condition in which the pupils of the eyes are different sizes. It is usually harmless and can be caused by a variety of factors, including medications, eye trauma, and neurological disorders....

ANK3-related intellectual disability-sleep disturbance syndrome is a rare genetic disorder caused by mutations in the ANK3 gene. It is characterized by intellectual disability, sleep disturbances, and other neurological features such as seizures, ...

Ankyloblepharon filiforme adnatum-cleft palate syndrome (AFA-CP) is a rare genetic disorder characterized by the fusion of the eyelids, cleft palate, and other facial abnormalities. It is caused by a mutation in the TP63 gene, which is responsible...

Ankyloblepharon filiforme adnatum-imperforate anus syndrome (AFA-IA) is a rare genetic disorder characterized by the fusion of the eyelids, imperforate anus, and other physical anomalies. It is caused by a mutation in the TP63 gene. Symptoms may i...

Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (AEC syndrome) is a rare genetic disorder characterized by the presence of ankyloblepharon (fusion of the eyelids), ectodermal defects (abnormalities of the skin, hair, nails, and teeth)...

Ankyloglossia, also known as tongue-tie, is a condition in which the lingual frenulum (the band of tissue that connects the bottom of the tongue to the floor of the mouth) is shorter than normal, restricting the movement of the tongue. This can ca...

Ankylosing spondylitis facts Ankylosing spondylitis belongs to a group of arthritis conditions that tend to cause chronic inflammation of the spine (spondyloarthropathies). Ankylosing spondylitis affects males two to three...

Ankylosing vertebral hyperostosis with tylosis is a rare condition that affects the spine and can cause the vertebrae to fuse together. It is characterized by the formation of bone spurs (osteophytes) on the vertebrae, which can lead to a narrowin...

Ankylostomiasis, also known as hookworm infection, is a parasitic infection caused by two species of hookworms, Ancylostoma duodenale and Necator americanus. It is most commonly found in tropical and subtropical regions, and is spread through cont...

Annular atrophic lichen planus is a rare form of lichen planus, a chronic skin condition that causes an itchy, scaly rash. It is characterized by round, atrophic (thinned) patches of skin with a raised, scaly border. The rash may be red, purple, o...

Annular epidermolytic ichthyosis is a rare genetic skin disorder that is characterized by thick, scaly patches of skin that form on the body. The patches are usually red and may be itchy or painful. The condition is caused by a mutation in the ker...