Dear colleagues!
Some CPS increase the risk of only one type of cancer, while others do so for various types of cancer. With the CPS Navigator, we want to provide you with information on which CPSs are associated with the cancer diagnoses listed below. If you, the physician, suspect the existence of a CPS in a patient with a specific cancer diagnosis, this instrument will make it easier for you to search for the most frequent and best-known CPS for this cancer diagnosis. The list does not claim to be exhaustive, especially since the findings in this area are constantly changing.
CPS-Navigator
Some cancer predisposition syndromes (CPS) increase the risk of only one type of cancer, while others do so for various types of cancer. With the CPS Navigator, we want to provide information which CPS are associated with the cancer diagnoses listed below. If you, the physician, suspect the existence of a CPS in a patient with a specific cancer diagnosis, this instrument will make it easier for you to search for the most frequent and best-known CPS for this cancer diagnosis. The list does not claim to be exhaustive, especially since the findings in this area are constantly changing.
| ANKRD26 Deficiency | |
| CEBPA Deficiency | |
| Dyskeratosis Congenita | |
| Fanconi Anemia | |
| GATA2 Deficiency | |
| Constitutional Mismatch Repair Deficiency | |
| Li-Fraumeni Syndrome | |
| RUNX1 Deficiency | |
| SAMD9 Deficiency | |
| SAMD9L Deficiency | |
| Severe Congenital Neutropenia | |
| Shwachman-Diamond Syndrome | |
| Trisomie 21 |
| BAP1 Tumor Predisposition Syndrome | |
| Gorlin Syndrome |
| APC-Associated Adenomatous Polyposis | |
| Juvenile Polyposis Syndrome | |
| Lynch Syndrome | |
| MUTYH-Associated Polyposis | |
| Constitutional Mismatch Repair Deficiency | |
| POLE Deficiency | |
| POLD1 Deficiency | |
| PTEN Harmatoma Tumor Syndrome | |
| Peutz-Jeghers Syndrome |
| KRAS Mutation | |
| Lynch Syndrome | |
| POLE Mutation | |
| PTEN Harmatoma Tumor Syndrome |
| Familiar Gastrointestinal Stromal Tumor | |
| Hereditary Pheochromocytoma/Paraganglioma Syndrome | |
| Neurofibromatosis Type 1 |
| Constitutional Mismatch Repair Deficiency | |
| L-2-Hydroxyglutaric Aciduria | |
| Li-Fraumeni Syndrome | |
| Lynch snydrome | |
| Neurofibromatosis Type 1 | |
| Noonan Syndrome | |
| Tuberous Sclerosis |
| ABCB11 (Intrahepatic Cholestasis) | |
| APC-Associated Adenomatous Polyposis | |
| CDKN2A Deficiency | |
| Glycogenosis Type 1 | |
| Glycogenosis Type 3 | |
| Prophyria | |
| Pyruvate Dehydrogenase Deficiency, Leigh Syndrome | |
| Ruijs-Aalsfs Syndrome | |
| Tyrosinemia Type 1 | |
| Fanconi Anemia |
| Carney Complex | |
| Peutz-Jeghers Syndrome |
| Ataxia Telangiectasia | |
| Bloom Syndrome | |
| Immunodeficiency Syndrome | |
| Constitutional Mismatch Repair Deficiency | |
| Nijmegen Breakage Syndrome |
| Ataxia-Telangiectasia | |
| BRCA1/2 mutation | |
| CDH1 mutation | |
| Fanconi anemia | |
| Li-Fraumeni Syndrome | |
| PALB2 mutation | |
| RAD51C/RAD51D mutation |
| BAP1 Tumor Predisposition Syndrome | |
| BRCA2 mutation | |
| CDK4 Deficiency | |
| CDKN2A Deficiency | |
| Dyskeratosis Congenita | |
| MITF Deficiency | |
| POLE Deficiency | |
| POT1 Deficiency | |
| Retinoblastoma Predisposition |
| Infantile Myofibromatosis |
| Carney Complex |
| Aneuploidy Syndrome | |
| Beckwith-Wiedemann Syndrome | |
| Bohring-Opitz Syndrome | |
| CTR9 Deficiency | |
| DICER1 Syndrome | |
| Fanconi Anemia | |
| Li-Fraumeni Syndrome | |
| Mulibrey (Muscle, Liver, Brain, and Eye) Nanism | |
| Perlman Syndrome | |
| REST Deficiency | |
| Simpson-Golabi-Behmel Syndrome | |
| Sotos Syndrome | |
| TRIM 28 mutation | |
| WT1-Associated Syndromes |
| IPMK Deficiency | |
| Multiple Endocrine Neoplasia Type 1 | |
| Neurofibromatosis Type 1 | |
| Tuberous Sclerosis | |
| Von Hippel-Lindau Syndrome |
| Hereditäre multiple Exostosen | |
| Li-Fraumeni Syndrome | |
| Retinoblastoma Predisposition | |
| Rothmund-Thomson Syndrome |
| Familial Isolated Pituitary Adenoma | |
| Multiple Endocrine Neoplasia Type 1 | |
| Carney Complex |
| BAP1 Tumor Predisposition Syndrome | |
| Birt-Hogg-Dubé Syndrome | |
| CDKN2B Deficiency | |
| Hereditary Leiomyomatosis and Renal Cell Cancer | |
| Hereditary Pheochromocytoma/Paraganglioma Syndrome | |
| MET Deficiency | |
| PBRM1 Deficiency | |
| PTEN Harmatoma Tumor Syndrome | |
| Tuberous Sclerosis | |
| Von Hippel-Lindau Syndrome |
| Carney Complex | |
| Neurofibromatosis Type 2 | |
| Schwannomatosis |
| Carney Complex | |
| DICER1 Syndrome |
| Tuberous Sclerosis |
| Trisomy 21 |
