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Dictionary » Hamartoma Syndrome, Multiple

Hamartoma Syndrome, Multiple

Introduction: Hamartoma Syndrome, Multiple

Description of Hamartoma Syndrome, Multiple

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

Hamartoma Syndrome, Multiple: Related Topics

These medical condition or symptom topics may be relevant to medical information for Hamartoma Syndrome, Multiple:

Terms associated with Hamartoma Syndrome, Multiple:

Terms Similar to Hamartoma Syndrome, Multiple:

Source - MeSH 2007

Broader terms for Hamartoma Syndrome, Multiple

Source - MeSH 2007

Hierarchical classifications of Hamartoma Syndrome, Multiple

The following list attempts to classify Hamartoma Syndrome, Multiple into categories where each line is subset of the next.

MeSH 2007 Hierarchy:

MeSH 2007 Hierarchy

MeSH 2007 Hierarchy

MeSH 2007 Hierarchy

Interesting Medical Articles:

Medical dictionaries:

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