Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome (AHUIDS) is a rare genetic disorder characterized by the absence of some or all of the fingers and toes (aphalangy), malformation of the vertebrae (hemivertebrae), malformation of t...

Aphalangy-syndactyly-microcephaly syndrome (ASM) is a rare genetic disorder characterized by the absence of some or all of the fingers and toes (aphalangy), webbing of the fingers and toes (syndactyly), and a small head size (microcephaly). It is ...

Aphasia, a disturbance in the formulation and comprehension of language, is due to damage to brain tissue areas responsible for language; aphasia may occur suddenly or develop over time, depending on the type and location of brain tissue damage....

Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome is a rare genetic disorder that affects multiple systems of the body. It is characterized by aphonia (loss of voice), deafness, retinal dystrophy (degeneration of t...

Sutton disease II is characterized by the recurring eruption of painful inflamed ulcers in the mouth (stomatitis). There may be multiple ulcers of varying sizes. These ulcers in the mouth are commonly called canker sores. Sutton disease II is also...

Canker sores are small, painful ulcers on the inside of the mouth, lips, or throat. Symptoms of canker sores include small, painful, crater-like ulcers. See a doctor if canker sores are accompanied by fever, last more than...

Aplasia Cutis Congenita is a rare disorder with a complicated pattern of inheritance. Babies are born with the absence of certain layer(s) of skin, most often on the scalp, but also on the trunk, and/or arms and legs. The affected area is typicall...

Aplasia cutis congenita (ACC) is a rare congenital disorder characterized by the absence of skin at birth. It is usually seen as a localized defect on the scalp, but can also occur on other parts of the body. The cause of ACC is unknown, but it is...

Aplasia cutis congenita-intestinal lymphangiectasia syndrome is a rare genetic disorder characterized by the absence of skin (aplasia cutis congenita) at birth, intestinal lymphangiectasia, and a variety of other symptoms. Intestinal lymphangiecta...

Aplasia cutis-myopia syndrome is a rare genetic disorder characterized by the absence of skin (aplasia cutis) on the scalp and/or forehead, and myopia (nearsightedness). It is caused by a mutation in the PAX6 gene, which is responsible for the dev...

Aplasia of lacrimal and salivary glands is a rare congenital disorder in which the lacrimal and salivary glands do not develop properly. This condition can cause dry eyes and dry mouth, as well as difficulty swallowing and speaking. In some cases,...

Aplastic anemia is a rare and serious condition in which the body's bone marrow does not produce enough new blood cells. This can lead to a shortage of red blood cells, white blood cells, and platelets. Symptoms of aplastic anemia include fatigue,...

Aplastic anemia-intellectual disability-dwarfism syndrome is a rare genetic disorder characterized by aplastic anemia (a condition in which the body does not produce enough new blood cells), intellectual disability, and dwarfism. It is caused by a...

Apnea of prematurity is a condition in which premature babies stop breathing for short periods of time. It is caused by an immature respiratory system and can be a sign of other health problems. It is usually treated with oxygen and/or medication....

Apnea, infantile is a condition in which an infant stops breathing for a period of time. It is most common in premature babies, but can also occur in full-term infants. Symptoms of infantile apnea include pauses in breathing, shallow breathing, an...

Apodia is a software platform designed to help businesses manage their customer relationships. It provides a suite of tools to help businesses track customer interactions, manage customer data, and automate customer service processes. Apodia also ...

Apolipoprotein A-I deficiency is a rare genetic disorder that affects the body's ability to metabolize fats. It is caused by a mutation in the APOA1 gene, which is responsible for producing the apolipoprotein A-I protein. This protein is essential...