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DeCS
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Descriptor English:
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Hamartoma Syndrome, Multiple
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Descriptor Spanish:
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síndrome de hamartomas múltiples
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Descriptor Portuguese:
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Síndrome do Hamartoma Múltiplo
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Synonyms English:
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Bannayan Riley Ruvalcaba Syndrome
Bannayan Zonana Syndrome
Bannayan-Riley-Ruvalcaba Syndrome
Bannayan-Ruvalcaba-Riley Syndrome
Bannayan-Zonana Syndrome
Cerebellum Dysplastic Gangliocytoma
Cerebellum Dysplastic Gangliocytomas
Cowden Disease
Cowden Syndrome
Cowden's Disease
Cowden's Syndrome
Cowdens Disease
Cowdens Syndrome
Dysplastic Gangliocytoma of Cerebellum
Dysplastic Gangliocytoma of the Cerebellum
Hamartoma Syndromes, Multiple
Lhermitte Duclos Disease
Lhermitte-Duclos Disease
Macrocephaly, Multiple Lipomas, and Hemangiomata
Macrocephaly, Pseudopapilledema, and Multiple Hemangiomas
Macrocephaly, Pseudopapilledema, and Multiple Hemangiomata
Multiple Hamartoma Syndrome
Multiple Hamartoma Syndromes
Myhre Riley Smith Syndrome
Myhre-Riley-Smith Syndrome
PTEN Hamartoma Tumor Syndrome
Riley Smith Syndrome
Riley-Smith Syndrome
Ruvalcaba Myhre Smith Syndrome
Ruvalcaba-Myhre Syndrome
Ruvalcaba-Myhre-Smith Syndrome
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Tree Number:
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C04.445.435
C04.651.435
C04.700.435
C16.320.700.435
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Definition English:
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A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE. |
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History Note English:
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91(87); was see under NEOPLASMS, MULTIPLE PRIMARY 1987-90
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Allowable Qualifiers English:
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Record Number:
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19179
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Unique Identifier:
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D006223
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Occurrence in VHL:
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Similar:
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DeCS
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