Diseases

Exostoses- multiple

Hereditary multiple exostoses (HME) is characterized by growths of multiple exostoses, benign cartilage-capped bone tumors that grow outward from the metaphyses of long bones. Exostoses can be associated with a reduction in skeletal growth, bony deformity, restricted motion of joints, shortened stature, premature osteoarthrosis, and compression of peripheral nerves. The median age of diagnosis is three years; nearly all affected individuals are diagnosed by twelve years of age. The risk for malignant degeneration to osteochondrosarcoma increases with age, although the lifetime risk of malignant degeneration is low (~1%).

Exostoses- multiple- type 1

Exostoses, multiple, type 1: Multiple extoses is a rare condition involving abnormal bone growths that occurs on bones. Type I differs from type II and III in the location of the genetic defect that causes the disorder. Type I tends to involve more bone growths and shorter arm and leg bones.

Exostoses- multiple- type 2

Exostoses, multiple, type 2: Multiple extoses is a rare condition involving abnormal bone growths that occurs on bones. Type II differs from type I and III in the location of the genetic defect that causes the disorder. Type I tends to be less severe than type I.

Exostoses- multiple- type 3

Exostoses, multiple, type 3: Multiple extoses is a rare condition involving abnormal bone growths that occurs on bones. Type II differs from type I and III in the location of the genetic defect that causes the disorder. Type I tends to be less severe than type I.

Exstrophy of the bladder

Bladder exstrophy, more properly, the exstrophy-epispadias complex is a rare congenital anomality occurring once every 40,000-50,000 live births with a 2:1 male:female ratio. The diagnosis involves a spectrum of anomalies of the lower abdominal wall, bladder, anterior bony pelvis, and external genitalia. It occurs due to failure of the abdominal wall to close during fetal development and results in protrusion of the posterior bladder wall through the lower abdominal wall.

Exstrophy of the bladder-epispadias

Exstrophy of the bladder is a complex combination of disorders that occurs during fetal development. The disorder usually involves many systems in the body, including the urinary tract, skeletal muscles and bones, and the digestive system. Bladder exstrophy means that the bladder is essentially inside out and exposed on the outside of the abdomen. Because the bladder and other structures are exposed to the outside of the body, urine constantly trickles onto the skin causing local irritation.

Exsudative retinopathy familial- X-linked- recessive

A rare progressive eye disorder which is inherited in a recessive X-linked manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function. The disorder is caused by a genetic defect on chromosome 11q14-q21 and the severity of the condition.

Exsudative retinopathy- familial

Familial exsudative vitreo-retinopathy (FEVR) or autosomal dominat exsudative vitreo-retinal degeneration (Criswick-Schepens, 1969) is an often overlooked disease, that commonly effects children but more seldom effects also

Extragonadal Germ Cell Tumor

Germ cells are primitive cells within the body that normally mature into ova (egg) or sperm cells. More than 90% of all germ cell tumors are gonadal; that is, they develop in the ovaries or the testes (the gonads). The remaining 5–10% of germ cell tumors arise outside of the gonads: these are the extragonadal germ cell tumors. These tumors occur mostly in the chest, lower back, and head.

Extrapulmonary Neuroendocrine Carcinoma

Extrapulmonary neuroendocrine carcinoma (EP-NEC) is a rare and aggressive form of cancer that can arise in various organs outside the lungs. These tumors are characterized by their high-grade features and neuroendocrine differentiation, meaning they share characteristics with neuroendocrine tumors found in the lung, but occur in other parts of the body. EP-NECs are known for their aggressive behavior, including rapid growth and potential for early metastasis. 

Exudative vitreoretinopathy 1

Abnormal vascularization of the peripheral retina and retinal detachment are the common clinical characteristics of Norrie disease pseudoglioma (NDP), Familial exudative vitreoretinopathy (FEVR), and Retinopathy of prematurity (ROP). NDP is a severe, X-linked recessive neurodevelopmental disorder affecting mostly males. But it can also affect female carriers. It is also often associated with some form of mental retardation and progressive sensorineural deafness in the second decade of life. Additionally, it exhibits intrafamilial variability in the onset and severity and more complex phenotypes in some patients. FEVR is a rare bilateral eye disorder affecting full-term infants with a high penetrance and highly variable expressivity even within the same family.

Fabry disease

Fabry disease is an inherited disorder that results from the buildup of a particular type of fat in the body's cells, called globotriaosylceramide or GL-3. 
Fabry disease affects many parts of the body. Signs and symptoms may include episodes of pain, particularly in the hands and feet (acroparesthesias); clusters of small, dark red spots on the skin called angiokeratomas; a decreased ability to sweat (hypohidrosis); cloudiness of the front part of the eye (corneal opacity); and hearing loss. Potentially severe complications can include progressive kidney damage, heart attack, and stroke. Milder forms of the disorder may appear later in life and affect only the heart or kidneys. Fabry disease is caused by mutations in the GLA gene and is inherited in an X-linked manner. Treatment may include enzyme replacement therapy (ERT); pain medications, ACE inhibitors; and chronic hemodialysis or renal transplantation for end stage renal disease.

FACES syndrome

A rare syndrome characterized mainly by short stature, webbed fingers and toes and skeletal abnormalities.

Faciocardiorenal syndrome

A rare syndrome characterized by a variety of abnormalities such as kidney anomaly, mental retardation, unusual facial features, heart problems and joint problems. Infant death or stillbirth may occur in some cases.

Facioscapulohumeral muscular dystrophy 1a

An inherited muscle disease involving slowly progressive muscle weakness. The condition is characterized by the early involvement of facial and shoulder muscles. Muscle weakness then spreads to the pelvis and legs. The onset, severity and rate of progression is variable.

Factor 2 deficiency

Alternative Names: Hypoprothrombinemia; Prothrombin deficiency. Factor II deficiency is a blood clotting (coagulation) problem caused by a lack of a substance (prothrombin) that is needed for blod to clot.

Factor V deficiency

Alternative Names: Parahemophilia; Owren's disease Factor V deficiency is an inherited condition that affects the ability of the blood to clot.

Factor V Leiden thrombophilia

Factor V Leiden thrombophilia is a common genetic disorder that leads to a predisposition or increased chance to develop blood clots in the veins (venous thrombosis).

Factor X deficiency

Factor X deficiency is a rare condition that affects the blood's ability to clot. The severity of the condition and the associated signs and symptoms can vary significantly from person to person. Common features of factor X deficiency may include easy bruising, frequent nosebleeds, bleeding gums, blood in the urine, and prolonged bleeding after minor injuries. Affected women may also experience heavy menstrual bleeding and may have an increased risk for first trimester miscarriage. 

Acquired (non-inherited) factor X deficiency, which is the most common form of the condition, generally occurs in people with no family history of the condition. Acquired factor X deficiency has a variety of causes including liver disease, vitamin K deficiency, exposure to certain medications that affect clotting, and cancers.

The inherited form of factor X deficiency (congenital factor X deficiency) is caused by mutations in the F10 gene and is inherited in an autosomal recessive manner. Treatment aims to control bleeding through intravenous (IV) infusions of plasma or concentrates of clotting factors.

Congenital factor X deficiency is among the most rare factor disorders, affecting an estimated one individual per 500,000-1,000,000 population worldwide. Only 50 cases of congenital factor X deficiency have been documented worldwide. 

Factor XI deficiency- congenital

Factor XI deficiency, congenital: A rare inherited bleeding disorder characterized by a deficiency of a blood protein called Factor XI which is needed for the blood clotting process. The condition is generally quite mild but the severity of the condition is variable.

Factor XII deficiency

Factor XII deficiency is an inherited disorder with no symptoms. Factor XII is a protein involved in blood clotting. A deficiency of this factor does not cause abnormal bleeding in the affected person, but the blood takes longer than normal to clot in a test tube.

Factor XIII Deficiency

Factor XIII deficiency is a rare, genetic bleeding disorder characterized by deficiency of clotting factor XIII. Clotting factors are specialized proteins that are essential for the blood to clot properly. Specifically, individuals with factor XIII deficiency form blood clots like normal, but these clots are unstable and often break down, resulting in prolonged, uncontrolled bleeding episodes. Factor XIII also affects other processes in the body and is known to play a role in proper wound healing and pregnancy. The severity of factor XIII deficiency bleeds can vary greatly from one person to another. Some individuals may have only mild symptoms; other individuals may have severe, life-threatening bleeds. With early diagnosis and prompt treatment, the more serious bleeds of factor XIII deficiency can be avoided. FXIII consists of two subunits: subunit A and subunit B. Most of the Factor XIII deficiency states are caused by mutations in subunit A; very few have a mutation in subunit B. Factor XIII deficiency is inherited as an autosomal recessive disorder.

Source: NORD

Fairbank disease

Fairbank disease: A rare inherited disorder that affects the secondary growth centers of bones usually in the hips, knees and ankles and results in mild dwarfism.

Fallopian tube cancer

Fallopian tube cancer develops in the tubes that connect a woman's ovaries and uterus. It is very rare and accounts for only 1-2% of all gynecological cancers. 

Fallopian tube cancer occurs when normal cells in one or both tubes change and grow in an uncontrolled way, forming a mass called a tumor. Cancer can begin in any of the different cell types that make up the fallopian tubes. The most common type is called adenocarcinoma (a cancer of cells from glands). Leiomyosarcoma (a cancer of smooth muscle cells) and transitional cell carcinoma (a cancer of the cells lining the fallopian tubes) are more rare. 

While some fallopian tube cancers actually begin in the tubes themselves, fallopian tube cancer is more often the result of cancer spreading from other parts of the body to the tubes.