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Diseases

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Diseases

Ectodermal dysplasia

Health care; Diseases

A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterised by the presence of abnormalities at birth and involvement of both the ...

Thalassemia

Health care; Diseases

A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more haemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely ...

B-cell lymphoma

Health care; Diseases

A group of heterogeneous lymphoid tumours generally expressing one or more B-cell antigens or representing malignant transformations of B-lymphocytes.

T-cell lymphoma

Health care; Diseases

A group of heterogeneous lymphoid tumours representing malignant transformations of T-lymphocytes.

Pelizaeus-Merzbacher disease

Health care; Diseases

A rare, slowly progressive disorder of myelin formation. Subtypes are referred to as classic, congenital, transitional, and adult forms of this disease. The classic form is X-chromosome linked, has ...

Subacute sclerosing panencephalitis

Health care; Diseases

A rare, slowly progressive encephalitis caused by chronic infection with the measles virus. The condition occurs primarily in children and young adults, approximately 2-8 years after the initial ...

Hyperlipoproteinemia type III

Health care; Diseases

A rather uncommon form of familial hyperlipemia characterised by the presence of lipoproteins of abnormal composition. The main abnormal lipoproteins are called beta-VLDL and have a different ...

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