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Results 1 - 10 of 52 for Other acquired skin disease
  1. C3 glomerulopathy 
    ... example, people with dense deposit disease may have acquired partial lipodystrophy, a condition characterized by a lack of fatty (adipose) tissue under the skin in the upper part of the body. Additionally, some people with dense deposit disease develop a buildup of yellowish deposits called drusen ...
    https://medlineplus.gov/genetics/condition/c3-glomerulopathy - Genetics
  2. Darier disease 
    ... This dependence on the SERCA2 enzyme may make skin cells particularly vulnerable to changes in this enzyme.The linear form of Darier disease is caused by ATP2A2 gene variants that are acquired during a person's lifetime and are present ...
    https://medlineplus.gov/genetics/condition/darier-disease - Genetics
  3. Von Willebrand disease 
    ... caused by inherited gene variants (also called mutations). Acquired von Willebrand syndrome ... in adulthood. ...
    https://medlineplus.gov/genetics/condition/von-willebrand-disease - Genetics
  4. Factor V deficiency 
    ... leading to its inactivation. These cases are called acquired factor V deficiency and usually occur in individuals ... Manzato F, Guidi GC, Franchini M. Inherited and acquired factor V deficiency. Blood Coagul Fibrinolysis. 2011 Apr; ...
    https://medlineplus.gov/genetics/condition/factor-v-deficiency - Genetics
  5. Familial candidiasis 
    ... because their immune systems are impaired by a disease such as acquired immune ... Candida is present on the skin and mucous membranes of up to half the ...
    https://medlineplus.gov/genetics/condition/familial-candidiasis - Genetics
  6. Thrombotic thrombocytopenic purpura 
    ... two major forms of thrombotic thrombocytopenic purpura, an acquired (noninherited) form and a familial (inherited) form. The acquired form usually appears in late childhood or adulthood. ...
    https://medlineplus.gov/.../thrombotic-thrombocytopenic-purpura - Genetics
  7. Cutis laxa 
    ... skin. Most cases are inherited, but some are acquired, which means they do not appear to be ... laxa are often noticeable in infancy or childhood, acquired cutis laxa typically appears later in life. This ...
    https://medlineplus.gov/genetics/condition/cutis-laxa - Genetics
  8. Hemophilia 
    ... proteins.Another form of the disorder, known as acquired hemophilia, is not caused by inherited gene variants. ... or other soft tissues, usually beginning in adulthood. Acquired hemophilia results when the body makes specialized proteins ...
    https://medlineplus.gov/genetics/condition/hemophilia - Genetics
  9. Paroxysmal nocturnal hemoglobinuria 
    Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired (not inherited) disorder that leads to the premature death and impaired production of blood cells. The disorder affects red blood cells (erythrocytes), ...
    https://medlineplus.gov/.../paroxysmal-nocturnal-hemoglobinuria - Genetics
  10. Factor XI deficiency 
    ... mutations. In these cases, the condition is called acquired factor XI deficiency. It can be caused by ... is made primarily by cells in the liver, acquired factor XI deficiency can also occur as the ...
    https://medlineplus.gov/genetics/condition/factor-xi-deficiency - Genetics
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