Turcot syndrome
Disease Term | Disease ID | Gene Symbol | References |
---|---|---|---|
Turcot syndrome (disorder) | C0265325 | APC | 7661930 |
MSH6 | 9927034, 16000562, 24362816, 16283678, 18409202, 20442441, 17557300, 11809679, 23788249, 23483711, 17259933, 10763829, 9390556, 18030674, 15340263, 18593904 | ||
MLH1 | 24362816, 9927033, 21120944, 15139004, 18593904, 17594722, 20533529, 22753075, 10763829, 17440981, 11726306, 11809679, 22949387, 7661930, 11389087, 20442441, 11427529, 23788249, 9927034, 22692065, 16083711, 15340263, 17510385, 9500552, 23403630, 14762794, 21404117 | ||
MSH2 | 7550317, 15340263, 12549480, 23788249, 11809679, 20442441, 10763829, 16372347, 19101824, 24362816, 17601929, 18593904, 9927034, 23483711 | ||
PMS2 | 20442441, 11809679, 15077197, 28218421, 23483711, 17557300, 16204034, 9419979, 26691941, 10763829, 15340263, 16507833, 23788249, 18030674, 27435373, 28297620, 14574005, 9500552, 9927034, 25691505, 7661930, 26116798, 23629955, 27050224, 24362816 | ||
FBXO11 |