Related MeSH Hierarchy (7)
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Hemorrhagic Disorders » Hemostatic Disorders » Pseudoxanthoma Elasticum
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Skin Abnormalities » Pseudoxanthoma Elasticum
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Pseudoxanthoma Elasticum
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Connective Tissue Diseases » Pseudoxanthoma Elasticum
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Pseudoxanthoma Elasticum
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Pseudoxanthoma Elasticum
Diseases [C] » Cardiovascular Diseases [C14] » Vascular Diseases » Hemostatic Disorders » Pseudoxanthoma Elasticum
Description
An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE. MeSH
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Phase 4 Indicated Drugs (1)
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Phase 2 Indicated Drugs (4)
Organization Involved with Phase 4 Indications (1)
Organization Involved with Phase 2 Indications (9)
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