Begreppsinformation
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Skin and Connective Tissue Diseases
Skin Diseases
Sebaceous Gland Diseases
Sebaceous Gland Neoplasms
...
Metabolic Diseases
DNA Repair-Deficiency Disorders
Colorectal Neoplasms, Hereditary Nonpolyposis
Lynch Syndrome II
Neoplasms
Neoplastic Syndromes, Hereditary
Colorectal Neoplasms, Hereditary Nonpolyposis
Lynch Syndrome II
...
Genetic Diseases, Inborn
Neoplastic Syndromes, Hereditary
Colorectal Neoplasms, Hereditary Nonpolyposis
Lynch Syndrome II
...
Colonic Diseases
Colorectal Neoplasms
Colorectal Neoplasms, Hereditary Nonpolyposis
Lynch Syndrome II
...
Rectal Diseases
Colorectal Neoplasms
Colorectal Neoplasms, Hereditary Nonpolyposis
Lynch Syndrome II
...
Intestinal Neoplasms
Colorectal Neoplasms
Colorectal Neoplasms, Hereditary Nonpolyposis
Lynch Syndrome II
...
Intestinal Neoplasms
Colorectal Neoplasms
Colorectal Neoplasms, Hereditary Nonpolyposis
Lynch Syndrome II
Föredragen term
Muir-Torre Syndrome
Typ
-
Topical Descriptor
Överordnat begrepp
Användningsanmärkning
- A form of LYNCH SYNDROME II associated with cutaneous SEBACEOUS GLAND NEOPLASMS. Muir-Torre syndrome is also associated with other visceral malignant diseases include colorectal, endometrial, urological, and upper gastrointestinal neoplasms.
Anmärkning om ändringshistoria
- 2009
Termer på andra språk
-
finska
-
Muir-Torre
-
Muir-Torren syndrooma
-
svenska
URI
http://www.yso.fi/onto/mesh/D055653
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