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Disease list

No. Id Disease Disease int Tissue/Cell line PubmedID Study design
1 459 Gastrointestinal - 0 Alcoholic liver disease (ALD) - 0 colon sigmoideum 18162065 Patient study phenotype-control
2 460 Gastrointestinal - 0 Alcoholic liver disease (ALD) - 0 CACO-2 cell 18162065 Cell culture study
3 184 Cardiovascular - 0 Cardiomyopathy, hypertrophic - 0 heart 17525252 Patient study phenotype-control
4 209 Cardiovascular - 0 Cardiomyopathy, hypertrophic - 0 heart 17234972 Patient study phenotype-control
5 212 Cardiovascular - 0 Cardiomyopathy, hypertrophic - 0 heart 17498736 Patient study phenotype-control
6 214 Cardiovascular - 0 Cardiomyopathy, hypertrophic - 0 heart 17468766 Patient study phenotype-control
7 216 Cardiovascular - 0 Cardiomyopathy, hypertrophic - 0 atrium 17468766 Patient study phenotype-control
8 217 Cardiovascular - 0 Cardiomyopathy, hypertrophic - 0 ventriculus 17468766 Patient study phenotype-control
9 252 Cardiovascular - 0 Cardiomyopathy, hypertrophic - 0 heart 17108080 Patient study phenotype-control
10 326 Cardiovascular - 0 Cardiomyopathy, ischemic - 0 myocardium 17712037 Patient study phenotype-control
11 414 Cardiomyopathy, dilated - 115200 Cardiomyopathy, ischemic - 0 heart 18582896 Patient study phenotype-control
12 404 Cancer - 0 Cholangiocarcinoma - 0 KMCH cell 17404574 Cell culture study
13 443 Cancer - 0 Cholangiocarcinoma - 0 KMS-6 cell 17621267 Cell culture study
14 444 Cancer - 0 Cholangiocarcinoma - 0 KMCH cell 16762633 Cell culture study
15 445 Cancer - 0 Cholangiocarcinoma - 0 KMCH cell 17220301 Cell culture study
16 97 Gastrointestinal - 0 Chronic gastritis - 0 stomach 18328430 Patient study phenotype-control
17 253 Cardiovascular - 0 Congestive heart failure - 0 heart 17108080 Patient study phenotype-control
18 458 Cardiovascular - 0 Coronary artery disease - 0 endocardium 17401374 Patient study phenotype-control
19 591 Coronary artery disease - 0 peripheral blood 20524934 Patient study phenotype-control
20 417 Cowden disease - 158350 Cowden disease, with PTEN mutation - 0 B-lymphoblast 18460397 Patient study phenotype-control
21 418 Cowden disease - 158350 Cowden disease, without PTEN mutation - 0 B-lymphoblast 18460397 Patient study phenotype-control
22 419 Cowden-like syndrome - 158350 Cowden-like syndrome, with PTEN mutation - 0 B-lymphoblast 18460397 Patient study phenotype-control
23 420 Cowden-like syndrome - 158350 Cowden-like syndrome, without PTEN mutation - 0 B-lymphoblast 18460397 Patient study phenotype-control
24 313 Muscular - 0 Dermatomyositis - 0 muscle 17942673 Patient study phenotype-control
25 526 Cancer - 0 Embryonal tumors with abundant neuropil and true rosettes (ETANTR) - 0 cerebellum 19057917 Patient study phenotype-control
26 631 Endometriosis - 0 19074548 Patient study phenotype-control
27 124 Ovarian cancer - 604370 Epithelial ovarian cancer - 0 ovary 17875710 Patient study phenotype-control
28 140 Ovarian cancer - 604370 Epithelial ovarian cancer - 0 ovary 18458333 Cell culture study
29 162 Ovarian cancer - 604370 Epithelial ovarian cancer - 0 ovary 18560586 Patient study phenotype-control
30 191 Ovarian cancer - 604370 Epithelial ovarian cancer - 0 OVCA-420 cell 18560586 Cell culture study