Free Online Database Of Diseases, Illnesses & Ailments


Here you can look through thousands of and diseases, ailments, medical conditions and illnesses. You can find the symptoms. Read about any ailment's diagnosis and find medications that can be used and the correct treatments that are needed.

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Diseases, Illnesses & Ailments Starting from Letter A

  1. Aagenaes syndrome
    Aagenaes syndrome is a condition which is characterized by inborn hypoplasia of the lymph vessels. This eventually causes recurring cholestasis on the formative years lymphedema on the legs. This could develop into hepatic cirrhosis and giant cell hepatitis (which could occur with portal tract fibrosis). The name of Aagenaes syndrome was derived from a pediatrician in Norway named Oystein Aagenaes. The name was finalized in 1968 when the condition was first described by Aagenaes. It is sometimes called cholestasis-lymphedema syndrome or simply CLS. [read more]

  2. Aarskog Ose Pande Syndrome
    Aarskog Ose Pande syndrome is a rare type of medical disorder where the main symptoms include lipodystrophy on the buttocks and face. Since this is an adipose tissue defect, the loss of body fat in the body could get severe and this state could progress extensively. There are three kinds of lipodystrophy: localized lipodystrophy, partial lipodystrophy and total lipodystrophy. One other symptom is Rieger anomaly. This anomaly is characterized by the absence or underdevelopment of teeth (it could also mean the delay of tooth eruption) and some abnormalities of the eyes and face. Having sparse hair is also a common sign. This does not only mean hair on one's head but also body hairs. Other defects include retardation of bone age and abnormal motion of the joints (which could eventually lead to dislocation). This syndrome could begin to affect the patient as early as the fetal stage. It could ruin the growth of the fetus in the uterus by slowing its development. When this happens, many other systems are affected. Development of the patient's skills on speech could also be delayed when this disorder is acquired. This and all other symptoms are similar to characteristics of many other diseases that is why the physician should perform a thorough checkup of the patient to be able to diagnose the real condition. Aarskog Ose Pande syndrome is also considered as a variant of Short syndrome. This symptom does not only mean having a short stature but also having low weight at birth and fat losses on the skin. [read more]

  3. Aarskog Syndrome
    Aarskog syndrome is an inherited disorder that is often characterized by abnormalities of the face, short stature, genital abnormalities and mucoloskeletal anomalies. [read more]

  4. Aase Smith syndrome (or Aase syndrome)
    Aase Smith syndrome also known as Aase syndrome is a very rare disorder that can be inherited. It is often characterized by skeletal and joint defects. Aase syndrome is known as an autosomal dominant condition. The genetic origin of the illness is still not known. Anemia which results from this syndrome is often caused by the underdevelopment of bone marrows. These bone marrows are where formation of blood cells takes place. The syndrome was named after two pediatricians who were David Weyhe Smith and Jon Morton Aase. [read more]

  5. Aase Syndrome
    Aase syndrome is a rare congenital defect characterized by anemia accompanied with certain skeletal deformities. [read more]

  6. Aaviophobia
    Aaviophobia is a fear of being on a plane while in flight. Other names include aviatophobia, aerophobia, and pteromerhanophobia. The condition is considered more of a symptom rather than a disease. When fear of flying reaches a level that can significantly interfere with a person's ability to travel by plane, it will then be classified as fear of flying. [read more]

  7. Abasia
    Abasia is a condition where the patient is unable to walk due to impaired muscle synchronization. This means that the patient lacks motor synchronization in walking. With this condition, the foundation of gait (this is the distance of the two feet when measured sideways) is not constant or cannot be measured. This often leads the patient to sway from side to side or in any other direction, nearly falls, only to recover in the end. There are many other medical conditions that are connected to this disorder: choreic abasia (brought about by chorea of the leg); paralytic abasia (this is a paralysis of the muscles in the legs); spastic abasia (a condition where the leg muscles stiffen because they do not coordinate properly); ataxic abasia (legs become ataxic); paroxysmal trepidant abasia (a condition where the legs become spastic); trembling abasia (by its name, it means trembling legs). Abasia often comes with astasis (this is the state of being unable to stand). This condition is also referred to as astasia-abasia. [read more]

  8. Abdominal Aortic Aneurysm
    Abdominal aortic aneurysm can be diagnosed on anyone but the most viable candidates are men aged over 60. Couple this range of age with some of the common risk factors and the patient is on his way to developing this condition. This disorder happens when a blood vessel enlarges abnormally or causes a protrusion. The abdominal aorta, which is a huge blood vessel, is the one responsible in supplying blood to the abdomen, the legs and the pelvic area. When this abdominal aortic aneurysm raptures, is truly becomes life-threatening and should be attended to immediately. [read more]

  9. Abdominal Cystic Lymphangioma
    Cystic lymphangioma is a very rare tumor (comprises just about 6% of tumors that are benign in children) which is often located in the axillary or cervical regions. Sometimes, there are exceptional cases where it is situated in the abdomen. When it is situated in the abdomen, it becomes a rare type of benign tumor which often appears in infants and some children under the age of 5. Boys are more vulnerable to this disease. Abdominal cystic lymphangioma happens when there is an inborn defect in the link of central connecting structure and the primary lymphatic channel. This manifests in abdominal tumors which could occur even without any compression from structures that are adjacent to that part. When clinically tested, these cysts appear as pseudo appendices or pseudo-ascites syndrome. [read more]

  10. Abdominal Defects
    Defects of the abdominal wall are comparatively common fetal abnormalities. It occurs in about 1 in every 2,000 births. Majority of these defects of the abdominal wall cannot be detected early on in pregnancy. When a defect is detected, it is necessary to pinpoint what type of defect it is so that proper medication and treatments can be done. There are many types of abdominal wall disorders. Some examples include: gastroschisis, omphalocele, esophageal atresia, and duodenal atresia. [read more]

  11. Abdominal Migraine
    Abdominal migraine is a kind of migraine commonly experienced by children. It is characterized by abdominal pain, vomiting and nausea. These migraines are thought to be present in the child's family members as well. [read more]

  12. Abdominal Pain
    Abdominal pain is is a medical condition that is characterized by the occurrence of the pain felt in the abdomen. [read more]

  13. Abercrombie Syndrome
    Abercrombie syndrome, also known as amyloid degeneration, is a progressive decay of the organ tissues due to the excessive amyloid infiltration that eats up the tissue fibers. It is sometimes known as waxy degeneration. [read more]

  14. Aberrant subclavian artery
    Aberrant subclavian artery is also known as the aberrant subclavian artery syndrome. This condition is a rare anatomical variety of the source of the left or the right subclavian artery. This abnormality has the most number of cases when it comes to the anomaly of inborn vascular aortic arch. The aberrant artery commonly occurs just distal on the left portion of the subclavian artery. It then passes later to the mediastinum when it is on its way to the upper right extremities. This course may be the root cause of a vascular ring about the mediastinal makeup. [read more]

  15. Abetalipoproteinemia
    Abetalipoproteinemia is a rare hereditary disorder that hinders regular absorption of fact from digested food. Patients with the disease lack the vitamins A, D, E and K. [read more]

  16. Ablepharon macrostomia syndrome
    Ablepharon macrostomia syndrome or AMS is a very uncommon genetic disorder that can be inherited. This syndrome is characterized by various physical defects which usually affect areas of the face, fingers, skin, and the genitalia (penis symptoms and some defects on the testes). Patients of AMS could also have other malformations on their abdominal walls or on their nipples. Other traits include having underdeveloped eyelids (or Ablepharon); the absence of eyebrows and eyelashes; mouths that look like that of a fish's (also known as Macrostomia); cracked skin; ears that appear to be low-set (also known as pinnae). The eye defects could appear due to ablepharon. Some people with AMS could also have very thin or sparse hair (alopecia); their skin appears to be wrinkled, dry, coarse, or thick; their fingers could also be webbed and with inadequate extension; the genitalia could have external malformations. In very few cases of Ablepharon macrostomia syndrome, the patient could have little or no nipples at all (having small nipples is known as hypoplastic nipples). One of the worst characteristics could be the protrusion of some parts of the large intestine through a dilated portion of the abdominal wall (this condition is called ventral or abdominal hernia). Infants and children who suffer from AMS may have some delays on the development of their language skills. Some of them may manifest signs of mild retardation of the mind while others may grow up to be normal. A disorder that appears to have the same features as Ablepharon macrostomia syndrome is the Barber-say syndrome. The latter is characterized by laxity of the skin; ablepharon; hypertelorism, macrostomia, telecanthus, acute hirsutism, and helix agenesis of the pair of ears. Less common signs of AMS include undescended testes and hernia on the umbilicus. [read more]

  17. Abnormal Uterine Bleeding
    Abnormal uterine bleeding refers to the excessive flow of blood during menstruation. The common symptoms of this condition are a massive menstrual discharge accompanied by pain in the lower abdomen. [read more]

  18. Abscess
    Abscess is a collection of pus or dead neutrophils that has mount up in a cavity made by the tissue on the basis of an infectious process or other foreign materials. [read more]

  19. Abscess Bartholin
    Abscess, bartholin (Bartholin's abscess) is characterized by the accumulation of pus that results in the formation of a lump or swelling in one of the Batholin glands, which are located on each side of the vaginal opening. [read more]

  20. Absence Seizure
    Absence seizure is more commonly known as the petit mal seizure that involves some a brief episodes or some sudden lapse of conscious activity. This occurs most often in children. Absence seizure may often look like the individual is only staring into space for a several seconds. This means in comparison to the regular epileptic seizures, the petit mal is very mild. However, some people may suffer from hundreds of episodes a day, which interrupts ordinary activities. [read more]

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