Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Término preferido
Gardner Syndrome
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Tipo
-
mesh:Descriptor
Definición
- A variant of ADENOMATOUS POLYPOSIS COLI caused by mutation in the APC gene (GENES, APC) on CHROMOSOME 5. It is characterized by not only the presence of multiple colonic polyposis but also extracolonic ADENOMATOUS POLYPS in the UPPER GASTROINTESTINAL TRACT; the EYE; the SKIN; the SKULL; and the FACIAL BONES; as well as malignancy in organs other than the GI tract.
Concepto genérico
Etiquetas alternativas
- Gardner's Syndrome
En otras lenguas
-
francés
-
Syndrome de Gardner et Richards
URI
http://data.loterre.fr/ark:/67375/JVR-FL20M1TM-3
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