| Descriptor English: | Hamartoma Syndrome, Multiple | ||||||
| Descriptor Spanish: |
Síndrome de Hamartoma Múltiple
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| Descriptor Portuguese: | Síndrome do Hamartoma Múltiplo | ||||||
| Descriptor French: | Syndrome des hamartomes multiples | ||||||
| Entry term(s): |
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(s): |
C04.445.435 C04.651.435 C04.700.435 C16.320.700.435 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D006223 | ||||||
| Scope note: | 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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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Hamartoma (1966-1986) Neoplasms, Multiple Primary (1966-1986) |
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| Public MeSH Note: | 91; was see under NEOPLASMS, MULTIPLE PRIMARY 1987-90 |
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| History Note: | 91(87); was see under NEOPLASMS, MULTIPLE PRIMARY 1987-90 |
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| DeCS ID: | 19179 | ||||||
| Unique ID: | D006223 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1986/06/23 | ||||||
| Revision Date: | 2018/06/29 |
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DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms
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Hamartoma Syndrome, Multiple
- Preferred
Lhermitte-Duclos Disease
- Related but not broader or narrower
PTEN Hamartoma Tumor Syndrome
- Related but not broader or narrower
Bannayan-Riley-Ruvalcaba Syndrome
- Related but not broader or narrower
| Concept UI |
M0009775 |
| Scope note | 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. |
| Preferred term | Hamartoma Syndrome, Multiple |
| Entry term(s) |
Cowden Disease Cowden Syndrome Cowden's Disease Cowden's Syndrome Cowdens Disease Cowdens Syndrome Hamartoma Syndromes, Multiple Multiple Hamartoma Syndrome Multiple Hamartoma Syndromes |
| Concept UI |
M0499747 |
| Preferred term | Lhermitte-Duclos Disease |
| Entry term(s) |
Cerebellum Dysplastic Gangliocytoma Cerebellum Dysplastic Gangliocytomas Dysplastic Gangliocytoma of Cerebellum Dysplastic Gangliocytoma of the Cerebellum Lhermitte Duclos Disease |
| Concept UI |
M0499746 |
| Preferred term | PTEN Hamartoma Tumor Syndrome |
| Concept UI |
M0499748 |
| Preferred term | Bannayan-Riley-Ruvalcaba Syndrome |
| Entry term(s) |
Bannayan Riley Ruvalcaba Syndrome Bannayan Zonana Syndrome Bannayan-Ruvalcaba-Riley Syndrome Bannayan-Zonana Syndrome Macrocephaly, Multiple Lipomas, and Hemangiomata Macrocephaly, Pseudopapilledema, and Multiple Hemangiomas Macrocephaly, Pseudopapilledema, and Multiple Hemangiomata Myhre Riley Smith Syndrome Myhre-Riley-Smith Syndrome Riley Smith Syndrome Riley-Smith Syndrome Ruvalcaba Myhre Smith Syndrome Ruvalcaba-Myhre Syndrome Ruvalcaba-Myhre-Smith Syndrome |
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