All diseases

55 entries on 1 page. Showing entries 1 - 55.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00003 - cancer, bladder 109800 15 15 MLH3, MSH3 - -
00005 - cancer, endometrial 608089 196 165 MLH3, MSH3 - -
00006 - Esophageal cancer 133239 8 0 MLH3, MSH3 - -
00007 - cancer, ovarian 167000 51 22 MLH3, MSH3 fallopian tube;ovary -
00008 - in vitro - 1213 1140 MSH3 - -
00009 - other - 227 225 MLH3, MSH3 - -
00011 - cancer, rectal - 56 53 FBXO11, MLH3, MSH3, MUTYH rectum -
00013 - cancer, breast - 92 83 FBXO11, MLH3, MSH3, MUTYH breast -
00014 - cancer, brain - 16 17 FBXO11, MLH3, MSH3, MUTYH brain -
00016 - neoplasia, colorectal, early onset - 12 12 FBXO11, MLH3, MSH3, MUTYH - -
00017 - cancer - 79 77 FBXO11, MLH3, MSH3, MUTYH - -
00019 - lymphoma - 0 0 FBXO11, MLH3, MSH3, MUTYH - -
00021 - cancer, skin, squamous cell carcinoma - 0 0 MLH3, MSH3 - -
00022 - Medulloblastoma 155255 2 3 MLH3, MSH3 - -
00024 - adenoma - 77 75 FBXO11, MLH3, MSH3, MUTYH - -
00025 - glioma, malignant - 8 8 MLH3, MSH3 - -
00026 - in silico - 1819 1818 MLH3, MSH3 - -
00028 - cancer, pancreatic 260350 6 6 FBXO11, MLH3, MSH3, MUTYH - -
00030 - cancer, prostate 176807 20 18 - prostate -
00031 - cancer, kidney - 17 17 - kidney -
00032 - cancer, skin - 11 11 - skin -
00033 - neoplasia, colorectal - 7 5 - - -
00049 - Adrenocortical carcinoma, hereditary 202300 1 1 - - -
00050 - polyp - 3 3 - - -
00010 ? unknown/not specified - 8798 898 FBXO11, MLH3, MSH3, MUTYH, POLD1, POLE - -
00036 ? unclassified / mixed - 165 164 - - -
00042 AFAP adenomatous polyposis, familial, attenuated (AFAP) - 0 0 - - -
00023 AML leukemia, myeloid, acute (AML) 601626 15 1 MLH3, MSH3 - -
00043 cancer, colon cancer, colon - 176 174 - - -
00045 cancer, duodenal cancer, duodenal - 2 2 - - -
00027 cancer, gastric cancer, gastric (neoplasm of stomach) 613659 11 10 MLH3, MSH3, MUTYH - -
00044 cancer, head and neck cancer, head and neck - 7 7 - - -
00039 cancer, liver cancer, hepatocellular 114550 0 0 - - -
00047 cancer, lung cancer, lung - 27 26 - - -
00048 cancer, oesophageal cancer, oesophageal - 1 1 - - -
00051 carcinoma carcinoma - 3 3 - - -
00029 CML leukemia, myeloid, chronic (CML) 608232 1 0 - - -
00002 CRC cancer, colorectal (CRC) 114500 2322 1618 MLH3, MSH3 - -
00055 CWS Cowden syndrome (CWS) 158350 10 10 - - -
00035 DIAR-5 diarrhea, type 5, with tufting enteropathy, congenital (DIAR-5) 613217 1 1 - - -
00041 FAP adenomatous polyposis, familial (FAP) - 1 1 - - -
00004 FAP-1 adenomatous polyposis, familial, type 1 (FAP-1, Gardner syndrome) 175100 4403 4402 APC - -
00038 HDD desmoid disease, hereditary 135290 0 0 - - -
00034 HNPCC-8 cancer, colorectal, nonpolyposis, hereditary, type 8 (HNPCC-8) 613244 0 0 - - -
00053 JPS polyposis syndrome, juvenile (JPS) 174900 6 6 - - -
00046 leukemia leukemia - 4 4 - - -
00001 Lynch Syndrome cancer, colorectal, nonpolyposis, hereditary, type 1 (Lynch syndrome, HNPCC-1) 120435 1374 432 EPCAM, MLH1, MLH3, MSH2, MSH3, MSH6, PMS2 - -
00037 MINAS neoplasia, multiple inherited alleles (MINAS) - 8 7 FBXO11, MLH3, MSH3, MUTYH, POLD1, POLE - -
00040 MMRCS cancer syndrome, mismatch repair (MMRCS) 276300 4 1 - - -
00012 MRTES Muir-Torre Syndrome 158320 71 3 FBXO11, MLH3, MSH3, MUTYH - -
00020 NF-1 neurofibromatosis, type 1 (NF-1) 162200 1 1 - - -
00052 PJS Peutz-Jeghers syndrome (PJS) 175200 4 4 STK11 - -
00015 polyposis polyposis - 110 100 FBXO11, MLH3, MSH3, MUTYH, POLD1, POLE - -
00018 polyps polyps - 295 292 FBXO11, MLH3, MSH3, MUTYH - -
00054 SSPCS Sessile Serrated Polyposis Cancer Syndrome 617108 2 2 - - -