 |
 |
 |
 |
|
| Please click here for english information | |
 |
|
 |
|
 |
|
 |
|
 |
|
 |
|
 |
|
 |
|
 |
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
| Onkologie |
| Multiple endokrine
Neoplasie Typ 1 (MEN 1-Gen, MIM 131100) |
| Multiple endokrine
Neoplasie Typ 2 (RET-Protooncogen, MIM 171400) |
| Multiple Pheochromocytoma,
Paraganglioma (Succinat Dehydrogenase Subunit D, SDHD-gen, MIM 602690; Succinat Dehydrogenase Subunit B, SDHB-gen, MIM 185470) |
| Hereditäres non-polyposis Colon-Carcinom, HNPCC (Mikrosatelliten-Instabilität) |
| Li Fraumeni-Syndrom (Tumorsuppressor-Gen p53, TP53, MIM191170) |
| Peutz-Jeghers
Syndrom (Hamartomatöses Polyposis-Syndrom, Serin/Threonin Proteinkinase 11-gen, PJS, MIM602216) |
| Neurofibromatose
Typ 1 (Neurofibromin-Gen, NF1, MIM 162200) |
| HPT-Jaw Tumor
Syndrom (HRTP2, Parafibromin-Gen, MIM 145001) |
| Von Hippel-Lindau-Syndrom (VHL-Gen, MIM 193300) |
2003 © BioGlobe
GmbH
|