Descriptor English: | Lynch Syndrome II | ||||||
Descriptor Spanish: |
Síndrome de Lynch II
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Descriptor Portuguese: | Síndrome de Lynch II | ||||||
Descriptor French: | Syndrome de Lynch de type II | ||||||
Entry term(s): |
Colon Cancer, Familial Nonpolyposis, Type 2 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 Lynch Cancer Family Syndrome II Lynch cancer family syndrome 2 |
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Tree number(s): |
C04.700.250.500 C16.320.700.250.500 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D055847 | ||||||
Scope note: | Hereditary nonpolyposis colorectal neoplasms associated with other malignancies, more commonly of ovarian or uterine origin. When also associated with SEBACEOUS GLAND NEOPLASMS, it is called MUIR-TORRE SYNDROME. |
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Allowable Qualifiers: |
BL blood BS blood supply CF cerebrospinal fluid CH chemistry CI chemically induced CL classification 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 SC secondary SU surgery TH therapy UL ultrastructure UR urine VE veterinary VI virology |
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Previous Indexing: |
Colorectal Neoplasms, Hereditary Nonpolyposis (1986-2008) |
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Public MeSH Note: | 2009; see COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS 1992-2008 |
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History Note: | 2009; use COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS 1992-2008 |
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DeCS ID: | 53061 | ||||||
Unique ID: | D055847 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 2009/01/01 | ||||||
Date of Entry: | 2008/07/08 | ||||||
Revision Date: | 2013/07/08 |
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DISEASES
Neoplasms [C04]Neoplasms
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Lynch Syndrome II
- Preferred
Concept UI |
M0004836 |
Scope note | Hereditary nonpolyposis colorectal neoplasms associated with other malignancies, more commonly of ovarian or uterine origin. When also associated with SEBACEOUS GLAND NEOPLASMS, it is called MUIR-TORRE SYNDROME. |
Preferred term | Lynch Syndrome II |
Entry term(s) |
Colon Cancer, Familial Nonpolyposis, Type 2 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 Lynch Cancer Family Syndrome II Lynch cancer family syndrome 2 |
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