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Hamartoma Syndrome, Multiple
Definition: A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Papules of the face and oral mucosa are the most characteristic lesion. Other changes occur in the skin, in the thyroid, the breast, the gastrointestinal system, and the nervous system.

Synonym(s): Cowden's Disease / Multiple Hamartoma Syndrome / Cowden Disease / Cowdens Disease / Disease, Cowden / Disease, Cowden's / Syndrome, Multiple Hamartoma
MeSH 2010 © U.S. National Library of Medicine®.
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  Web resources for "Hamartoma Syndrome, Multiple"
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view the HON description of the site HONcode - Cowden syndrome - Genetics Home Referenceghr.nlm.nih.gov  
 
 

Broader term(s): - Hamartoma - Neoplasms - Neoplastic Syndromes, Hereditary

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  Medical image(s) for "Hamartoma Syndrome, Multiple"
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Broader term(s): - Hamartoma - Neoplasms
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  Medical News for "Hamartoma Syndrome, Multiple"
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Broader term(s): - Neoplasms

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  Scientific articles from MEDLINE for "Hamartoma Syndrome, Multiple"
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Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy

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  Clinical Trials for "Hamartoma Syndrome, Multiple"
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Broader term(s): - Hamartoma - Neoplasms

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Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy


  Broader term(s):
      Diseases
          Congenital, Hereditary, and Neonatal Diseases and Abnormalities
              Genetic Diseases, Inborn
                  Neoplastic Syndromes, Hereditary 
      Diseases
          Neoplasms
              Neoplastic Syndromes, Hereditary 
              Neoplasms, Multiple Primary 
              Hamartoma 

MeSH 2010 © U.S. National Library of Medicine®.

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