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Hamartoma Syndrome, Multiple: 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.
Source: MeSH 2007
These medical condition or symptom topics may be relevant to medical information for Hamartoma Syndrome, Multiple:
Source - MeSH 2007
Source - MeSH 2007
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