MeSH term	Gene1/score	Gene2/score	Gene3/score	
MESH:D020167/Hyperlysinemias RPS6/0.414 MLH1/0.408 CHAF1A/0.408 
MESH:D013631/Tangier Disease CASP14/0.476 SLC39A14/0.476 INSIG1/0.476 
MESH:D017490/Ichthyosis, Lamellar RDH5/0.477 ACSS2/0.466 MEIS1/0.466 
MESH:D005211/Fascioliasis LPAR4/0.397 PPARGC1B/0.389 MLXIPL/0.388 
MESH:D007566/Jaundice, Chronic Idiopathic GDNF/0.412 LDHB/0.411 RAD51AP1/0.409 
MESH:D020391/Muscular Dystrophy, Facioscapulohumeral RARRES1/0.401 PAX3/0.385 KEAP1/0.382 
MESH:D055673/Acrocallosal Syndrome TTPA/0.386 IGFALS/0.378 PAWR/0.376 
MESH:D009221/Myositis Ossificans SDCBP/0.453 ENO3/0.451 TCN2/0.447 
MESH:D059446/Heterotaxy Syndrome POLE2/0.392 POLA2/0.369 PRSS23/0.369 
MESH:D056846/Weill-Marchesani Syndrome CENPM/0.211 AURKA/0.211 FAM83D/0.211 
MESH:D054880/Aspartylglucosaminuria EZH2/0.443 GNAI3/0.432 ATP6AP1/0.431 
MESH:D007715/Klippel-Trenaunay-Weber Syndrome SDCBP/0.454 HHIP/0.453 ENO3/0.453 
MESH:D006010/Glycogen Storage Disease Type III EZH2/0.486 KIF20A/0.484 CENPM/0.481 
MESH:D052497/Lipodystrophy, Congenital Generalized GDNF/0.411 OSM/0.402 PGAM2/0.402 
MESH:D066253/Vascular Remodeling ANGPTL4/0.489 MLXIPL/0.478 ABCD3/0.478 
MESH:D053306/Hyper-IgM Immunodeficiency Syndrome E2F2/0.259 RBL1/0.259 CCNF/0.259 
MESH:D016884/Polyendocrinopathies, Autoimmune HOXA11/0.319 PIK3IP1/0.319 SLC7A6/0.319 
MESH:D016511/Severe Combined Immunodeficiency ZEB1/0.214 HHIP/0.197 GLI2/0.197 
MESH:D050010/Hyperthyroxinemia, Familial Dysalbuminemic DNAJB11/0.306 LGR5/0.306 SLC39A6/0.306 
MESH:D005633/Fructose Intolerance EZH2/0.487 KIF20A/0.486 CENPM/0.483 
MESH:D016726/Plasma Cell Granuloma, Pulmonary DNAJB11/0.414 LGR5/0.414 SLC39A6/0.414 
MESH:D017824/Bone Cysts, Aneurysmal HTR6/0.412 GLA/0.411 LCT/0.411 
MESH:D017204/Angelman Syndrome E2F3/0.251 BLVRB/0.251 GNB2/0.251 
MESH:D017436/Kallmann Syndrome E2F2/0.371 RBL1/0.371 CCNF/0.371 
MESH:D057770/Hyalinosis, Systemic DNAJB11/0.345 LGR5/0.345 SLC39A6/0.345 
MESH:D010283/Paratuberculosis INHA/0.336 CAMKK2/0.336 LPAR4/0.336 
MESH:D063766/Pediatric Obesity ZEB1/0.481 HHIP/0.48 GLI2/0.48 
MESH:D052476/Hypobetalipoproteinemia, Familial, Apolipoprotein B DVL2/0.5 SRRD/0.5 DECR1/0.5 
MESH:D008072/Hyperlipoproteinemia Type I VIP/0.461 CD68/0.46 CENPM/0.458 
MESH:D016657/Cerebral Amyloid Angiopathy ADH1A/0.487 ADH5/0.487 CST3/0.487 
MESH:D012618/Sea-Blue Histiocyte Syndrome D2HGDH/0.483 DDX3X/0.483 MME/0.481 
MESH:D003528/Carcinoma, Adenoid Cystic PPARA/0.489 HMGCR/0.487 ALOX5AP/0.487 
MESH:D017044/Polycystic Kidney, Autosomal Recessive E2F2/0.369 RBL1/0.369 CCNF/0.369 
MESH:D013734/Androgen-Insensitivity Syndrome E2F2/0.43 RBL1/0.43 CCNF/0.43 
MESH:D020162/Hyperargininemia MAPK12/0.477 TP53I3/0.477 WRN/0.477 
MESH:D020788/Bardet-Biedl Syndrome NTM/0.376 DVL2/0.374 SRRD/0.374 
MESH:D007966/Leukodystrophy, Metachromatic MAPK12/0.484 TP53I3/0.484 PPP1R12A/0.484 
MESH:D009087/Mucopolysaccharidosis VI CENPM/0.466 AURKA/0.466 FAM83D/0.466 
MESH:D055577/Farber Lipogranulomatosis MAPK12/0.486 OGDH/0.486 TP53I3/0.486 
MESH:D056807/Argininosuccinic Aciduria MAPK12/0.478 TP53I3/0.478 WRN/0.478 
MESH:D017825/Canavan Disease HSPB8/0.402 ABL1/0.402 MT4/0.397 
MESH:D018234/Sarcoma, Alveolar Soft Part ARHGDIA/0.457 SLCO1B1/0.455 PTEN/0.455 
MESH:D020159/Citrullinemia MAPK12/0.48 TP53I3/0.48 WRN/0.48 
MESH:D017827/Machado-Joseph Disease INHBA/0.494 ACTG2/0.494 RBP3/0.493 
MESH:D018277/Carcinoma, Mucoepidermoid PKLR/0.474 COMTD1/0.474 COX15/0.473 
MESH:D018332/Nevus, Epithelioid and Spindle Cell STAT5A/0.499 YBX2/0.497 ITGA3/0.497 
MESH:D018980/Williams Syndrome E2F3/0.361 BLVRB/0.361 GNB2/0.361 
MESH:D008375/Maple Syrup Urine Disease RPS6/0.415 MLH1/0.409 CHAF1A/0.409 
MESH:D018211/Chondrosarcoma, Mesenchymal STAT5A/0.483 COX15/0.481 EIF2AK1/0.481 
MESH:D007888/Leigh Disease HSPB8/0.389 ALPI/0.386 MT4/0.384 
MESH:D009767/Obesity, Morbid M6PR/0.5 CFTR/0.5 CYP51A1/0.5 
MESH:D057826/Vitelliform Macular Dystrophy E2F2/0.386 RBL1/0.386 CCNF/0.386 
MESH:D020914/Myopathies, Structural, Congenital LPAR4/0.388 HOXA11/0.372 PIK3IP1/0.372 
MESH:D007947/Leukemia, Megakaryoblastic, Acute PPARA/0.49 HMGCR/0.489 ALOX5AP/0.489 
MESH:D001816/Bloom Syndrome DNAJB11/0.346 LGR5/0.346 SLC39A6/0.346 
MESH:D015465/Leukemia, Myeloid, Accelerated Phase CYBA/0.491 UCN2/0.49 CYP11B1/0.49 
MESH:D006223/Hamartoma Syndrome, Multiple UGT2B15/0.233 SCP2/0.227 HOXA11/0.21 
MESH:D065627/Familial Primary Pulmonary Hypertension SDCBP/0.455 HHIP/0.454 ENO3/0.454 
MESH:D065635/Benign Paroxysmal Positional Vertigo LPAR4/0.468 TTPA/0.458 PRKAA2/0.457 
MESH:D000564/Ameloblastoma DNAJB11/0.448 LGR5/0.448 SLC39A6/0.448 
MESH:D056685/Costello Syndrome E2F2/0.237 RBL1/0.237 CCNF/0.237 
MESH:D003397/Craniopharyngioma ARHGDIA/0.458 SLCO1B1/0.457 PTEN/0.457 
MESH:D008339/Mandibular Neoplasms CHST8/0.432 FOXA2/0.432 SDC3/0.432 
MESH:D009634/Noonan Syndrome PLTP/0.329 PTPN1/0.322 DHRS7/0.319 
MESH:D061325/Hereditary Breast and Ovarian Cancer Syndrome DHRS7/0.364 PDK4/0.361 RBP2/0.349 
MESH:D028921/Biotinidase Deficiency CENPM/0.476 AURKA/0.476 FAM83D/0.476 
MESH:D009958/Orofaciodigital Syndromes E2F2/0.409 RBL1/0.409 CCNF/0.409 
MESH:D000708/Anaplasia HOXA11/0.374 PIK3IP1/0.374 SLC7A6/0.374 
MESH:D002285/Carcinoma, Intraductal, Noninfiltrating PKLR/0.476 COMTD1/0.476 COX15/0.474 
MESH:D013103/Spherocytosis, Hereditary E2F2/0.412 RBL1/0.412 CCNF/0.412 
MESH:D057765/Eosinophilic Esophagitis MLXIPL/0.471 BSG/0.467 LPAR4/0.467 
MESH:D020642/Acatalasia EZH2/0.444 GNAI3/0.434 ATP6AP1/0.432 
MESH:D049288/Muscular Dystrophies, Limb-Girdle RARRES1/0.404 PAX3/0.388 KEAP1/0.384 
MESH:D006623/von Hippel-Lindau Disease LPAR4/0.389 HOXA11/0.375 PIK3IP1/0.375 
MESH:D017074/Common Variable Immunodeficiency DNAJB11/0.415 LGR5/0.415 SLC39A6/0.415 
MESH:D053307/Hyper-IgM Immunodeficiency Syndrome, Type 1 E2F2/0.42 RBL1/0.42 CCNF/0.42 
MESH:D000742/Anemia, Dyserythropoietic, Congenital E2F2/0.414 RBL1/0.414 CCNF/0.414 
MESH:D001506/Beckwith-Wiedemann Syndrome E2F2/0.326 RBL1/0.326 CCNF/0.326 
MESH:D007724/Vulvar Lichen Sclerosus PPARGC1B/0.487 MLXIPL/0.484 TCN2/0.483 
MESH:D010188/Exocrine Pancreatic Insufficiency DNAJB11/0.417 LGR5/0.417 SLC39A6/0.417 
MESH:D058747/CHARGE Syndrome DNAJB11/0.31 LGR5/0.31 SLC39A6/0.31 
MESH:D058627/Megalencephaly ABCD3/0.407 TTPA/0.397 PAWR/0.397 
MESH:D016864/Li-Fraumeni Syndrome DNAJB11/0.2 LGR5/0.2 SLC39A6/0.2 
MESH:D015794/Choroideremia E2F2/0.249 RBL1/0.249 CCNF/0.249 
MESH:D017034/Epilepsy, Frontal Lobe DVL2/0.496 SRRD/0.496 DECR1/0.496 
MESH:D007593/Joint Instability DNAJB11/0.418 LGR5/0.418 SLC39A6/0.418 
MESH:D019595/Severe Dengue MLXIPL/0.474 BSG/0.47 LPAR4/0.47 
MESH:D056733/Carney Complex KCNK9/0.372 COMTD1/0.369 GRIA3/0.368 
MESH:D007873/Legg-Calve-Perthes Disease TCN2/0.484 AXIN1/0.484 ABCD4/0.484 
MESH:D065708/Porencephaly PAX3/0.463 ACSS2/0.46 MEIS1/0.46 
MESH:D009394/Nephritis, Hereditary PPARGC1B/0.356 MLXIPL/0.356 PDK4/0.351 
MESH:D018230/Leiomyoma, Epithelioid DCX/0.489 STAT5A/0.489 SREBF2/0.489 
MESH:D016108/Epidermolysis Bullosa Dystrophica RDH5/0.394 S100A10/0.388 SMAD7/0.382 
MESH:D004062/DiGeorge Syndrome RDH5/0.463 E2F2/0.453 RBL1/0.453 
MESH:D057130/Leber Congenital Amaurosis PPARGC1B/0.364 UGT2B15/0.359 SCP2/0.359 
MESH:D058456/Retinal Telangiectasis LPAR4/0.391 PPARGC1B/0.386 BSG/0.381 
MESH:D012415/Rubinstein-Taybi Syndrome SCN4A/0.329 CCNC/0.325 E2F3/0.318 
MESH:D018365/Neoplasm, Residual HOXA11/0.378 PIK3IP1/0.378 SLC7A6/0.378 
MESH:D056730/Silver-Russell Syndrome E2F2/0.318 RBL1/0.318 CCNF/0.318 
MESH:D028243/Cerebral Amyloid Angiopathy, Familial ALPI/0.448 MAPK12/0.447 TP53I3/0.447 
MESH:D020252/Gastric Antral Vascular Ectasia LPAR4/0.441 HHIP/0.44 GLI2/0.44 
MESH:D018296/Pilomatrixoma CAMK2A/0.467 TRIB2/0.466 POLK/0.466 
MESH:D058631/Pycnodysostosis MVD/0.269 UBE2C/0.267 PRC1/0.267 
MESH:D055113/Chronic Periodontitis HP/0.49 PPARGC1B/0.489 TCN2/0.486 
MESH:D015818/Eye Infections, Bacterial LPAR4/0.384 CHST8/0.371 SDC3/0.371 
MESH:D006105/Granulomatous Disease, Chronic E2F2/0.374 RBL1/0.374 CCNF/0.374 
MESH:D058490/46, XY Disorders of Sex Development ANGPTL4/0.49 E2F2/0.49 RBL1/0.49 
MESH:D050035/Sexual Infantilism POLE2/0.45 KIF22/0.445 ANGPTL4/0.443 
MESH:D019294/Xanthomatosis, Cerebrotendinous GDNF/0.418 LDHB/0.412 RAD51AP1/0.411 
MESH:D004410/Dyslexia CYP26B1/0.5 PDK4/0.5 IFRD1/0.5 
MESH:D054221/Classical Lissencephalies and Subcortical Band Heterotopias PAX3/0.474 KEAP1/0.473 ACSS2/0.473 
MESH:D018208/Liposarcoma, Myxoid DHRS7/0.484 DCX/0.484 STAT5A/0.484 
MESH:D010580/Peutz-Jeghers Syndrome CHKA/0.296 TRIB3/0.282 COX15/0.279 
MESH:D017624/WAGR Syndrome RBP3/0.42 RBP1/0.42 RDH10/0.42 
MESH:D006627/Hirschsprung Disease POLE2/0.339 PRKAA2/0.319 SDCBP/0.316 
MESH:D019871/Dyskeratosis Congenita UBE2C/0.283 PRC1/0.283 CENPM/0.26 
MESH:D009477/Hereditary Sensory and Autonomic Neuropathies ANGPTL4/0.339 PRKAA2/0.307 SIRT2/0.295 
MESH:D054067/Dihydropyrimidine Dehydrogenase Deficiency EZH2/0.445 GNAI3/0.435 ATP6AP1/0.434 
MESH:D003811/Dentinogenesis Imperfecta POLE2/0.409 TCN2/0.401 AXIN1/0.401 
MESH:D012779/Short Rib-Polydactyly Syndrome POLE2/0.424 E2F2/0.422 RBL1/0.422 
MESH:D008065/Lipoid Proteinosis of Urbach and Wiethe DNAJB11/0.349 LGR5/0.349 SLC39A6/0.349 
MESH:D053358/Ectodermal Dysplasia 1, Anhidrotic RDH5/0.395 RETSAT/0.384 GATA6/0.376 
MESH:D053359/Ectodermal Dysplasia 3, Anhidrotic RDH5/0.427 KEAP1/0.422 RETSAT/0.422 
MESH:D053360/Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive RDH5/0.428 KEAP1/0.424 RETSAT/0.424 
MESH:D021921/Aortic Stenosis, Supravalvular PPARGC1B/0.481 MTR/0.481 MLXIPL/0.48 
MESH:D020389/Muscular Dystrophy, Emery-Dreifuss E2F3/0.362 BLVRB/0.362 GNB2/0.362 
MESH:D000567/Amelogenesis Imperfecta E2F2/0.473 RBL1/0.473 CCNF/0.473 
MESH:D044542/LEOPARD Syndrome POLE2/0.404 PAWR/0.394 UGCG/0.389 
MESH:D054069/Multiple Acyl Coenzyme A Dehydrogenase Deficiency CD68/0.352 RAD51AP1/0.349 RET/0.348 
MESH:D004613/Ellis-Van Creveld Syndrome RDH5/0.425 CGA/0.422 S100A10/0.421 
MESH:D005097/Exostoses, Multiple Hereditary SCN5A/0.379 CCNA1/0.375 RBP3/0.371 
MESH:D019280/Branchio-Oto-Renal Syndrome E2F2/0.328 RBL1/0.328 CCNF/0.328 
MESH:D005171/Factor X Deficiency E2F2/0.395 RBL1/0.395 CCNF/0.395 
MESH:D005173/Factor XI Deficiency E2F2/0.397 RBL1/0.397 CCNF/0.397 
MESH:D005175/Factor XII Deficiency E2F2/0.398 RBL1/0.398 CCNF/0.398 
MESH:D005177/Factor XIII Deficiency E2F2/0.399 RBL1/0.399 CCNF/0.399 
MESH:D005166/Factor V Deficiency E2F2/0.401 RBL1/0.401 CCNF/0.401 
MESH:D005168/Factor VII Deficiency E2F2/0.402 RBL1/0.402 CCNF/0.402 
MESH:D002836/Hemophilia B E2F2/0.381 RBL1/0.381 CCNF/0.381 
MESH:D054119/Arachnodactyly POLE2/0.417 TCN2/0.414 AXIN1/0.414 
MESH:D004479/Ectopia Lentis YBX2/0.302 EMC9/0.302 TPD52L2/0.302 
MESH:D015319/Fructose-1,6-Diphosphatase Deficiency EZH2/0.489 KIF20A/0.487 CENPM/0.484 
MESH:D057135/Wet Macular Degeneration PPARGC1B/0.49 TCN2/0.487 AXIN1/0.487 
MESH:D010485/Periapical Periodontitis LPAR4/0.466 BSG/0.464 MLXIPL/0.463 
MESH:D058165/22q11 Deletion Syndrome E2F2/0.339 RBL1/0.339 CCNF/0.339 
MESH:D049068/Plagiocephaly, Nonsynostotic E2F2/0.478 RBL1/0.478 CCNF/0.478 
MESH:D000130/Achondroplasia E2F2/0.407 RBL1/0.407 CCNF/0.407 
MESH:D013796/Thanatophoric Dysplasia E2F2/0.372 RBL1/0.372 CCNF/0.372 
MESH:D058494/Walker-Warburg Syndrome ACSS2/0.398 MEIS1/0.398 RBP3/0.368 
MESH:D058249/Birt-Hogg-Dube Syndrome DNAJB11/0.313 LGR5/0.313 SLC39A6/0.313 
MESH:D016112/Ichthyosis Vulgaris RDH5/0.369 UBE2C/0.352 PRC1/0.352 
MESH:D054091/Periventricular Nodular Heterotopia RARRES1/0.476 PAX3/0.47 KEAP1/0.468 
MESH:D007640/Keratoconus DNAJB11/0.42 LGR5/0.42 SLC39A6/0.42 
MESH:D056684/Yellow Nail Syndrome ARF5/0.221 ESRRA/0.221 FKBP4/0.221 
MESH:D058497/Fraser Syndrome YBX2/0.277 EMC9/0.277 TPD52L2/0.277 
MESH:D005645/Fucosidosis MAPK12/0.45 TP53I3/0.45 WRN/0.45 
MESH:D017250/Caliciviridae Infections DNAJB11/0.421 LGR5/0.421 SLC39A6/0.421 
MESH:D005953/Glycogen Storage Disease Type I EZH2/0.49 KIF20A/0.489 CENPM/0.486 
MESH:D000746/Anemia, Hemolytic, Congenital Nonspherocytic E2F2/0.415 RBL1/0.415 CCNF/0.415 
MESH:D005236/Favism E2F2/0.424 RBL1/0.424 CCNF/0.424 
MESH:D007965/Leukodystrophy, Globoid Cell SLC39A14/0.478 SS18L2/0.477 HOXC8/0.477 
MESH:D009085/Mucopolysaccharidosis IV CENPM/0.467 AURKA/0.467 FAM83D/0.467 
MESH:D056768/Giant Axonal Neuropathy SCN4A/0.378 E2F3/0.375 BLVRB/0.375 
MESH:D006011/Glycogen Storage Disease Type IV EZH2/0.491 KIF20A/0.49 CENPM/0.487 
MESH:D007714/Klippel-Feil Syndrome POLE2/0.319 YBX2/0.306 EMC9/0.306 
MESH:D046150/Laron Syndrome E2F2/0.261 RBL1/0.261 CCNF/0.261 
MESH:D006210/Hallermann's Syndrome E2F2/0.489 RBL1/0.489 CCNF/0.489 
MESH:D000794/Angiokeratoma DNAJB11/0.45 LGR5/0.45 SLC39A6/0.45 
MESH:D016537/Gangliosidosis, GM1 HDAC7/0.494 LMCD1/0.494 TRIP13/0.494 
MESH:D054975/Pallister-Hall Syndrome RBP3/0.432 RBP1/0.432 RDH10/0.432 
MESH:D049290/Tay-Sachs Disease, AB Variant HSPB6/0.499 RALA/0.499 CX3CL1/0.499 
MESH:D019339/Port-Wine Stain PLTP/0.378 PAWR/0.371 PPARGC1B/0.355 
MESH:D019080/Cafe-au-Lait Spots HHIP/0.441 GLI2/0.441 SUFU/0.441 
MESH:D005359/Fibrous Dysplasia, Polyostotic TCN2/0.499 SDCBP/0.499 AXIN1/0.499 
MESH:D011556/Pseudopseudohypoparathyroidism VIP/0.453 CD68/0.451 PSMC6/0.45 
MESH:D029461/Sialic Acid Storage Disease MAPK12/0.481 TP53I3/0.481 WRN/0.481 
MESH:D001606/Bernard-Soulier Syndrome E2F2/0.364 RBL1/0.364 CCNF/0.364 
MESH:D018887/Landau-Kleffner Syndrome TTPA/0.484 HHIP/0.484 GLI2/0.484 
MESH:D016538/Mucopolysaccharidosis VII CENPM/0.468 AURKA/0.468 FAM83D/0.468 
MESH:D002804/Chondroblastoma POLK/0.471 DNAJB11/0.471 LGR5/0.471 
MESH:D001656/Biliary Atresia YBX2/0.303 EMC9/0.303 TPD52L2/0.303 
MESH:D013661/Tay-Sachs Disease HSPB6/0.5 RALA/0.5 CX3CL1/0.5 
MESH:D012497/Sandhoff Disease HSPB6/0.497 RALA/0.497 CX3CL1/0.497 
MESH:D000474/Alkaptonuria EZH2/0.448 GNAI3/0.438 ATP6AP1/0.435 
MESH:D028922/Holocarboxylase Synthetase Deficiency CENPM/0.477 AURKA/0.477 FAM83D/0.477 
MESH:D010004/Osteoarthropathy, Primary Hypertrophic ARF5/0.267 ESRRA/0.267 FKBP4/0.267 
MESH:D010661/Phenylketonurias RPS6/0.417 MLH1/0.411 CHAF1A/0.411 
MESH:D007926/Lesch-Nyhan Syndrome BCR/0.365 PPP1R3C/0.362 GTF2H4/0.362 
MESH:D054000/Nevus, Sebaceous of Jadassohn PPOX/0.296 RAMP3/0.29 CMA1/0.29 
MESH:D004687/Enchondromatosis TCN2/0.489 AXIN1/0.489 ABCD4/0.489 
MESH:D016532/Mucopolysaccharidosis II TERF2/0.434 CALCB/0.434 MAPK12/0.432 
MESH:D008059/Mucopolysaccharidosis I CENPM/0.47 AURKA/0.47 FAM83D/0.47 
MESH:D018323/Hemangioendothelioma, Epithelioid PPARA/0.491 COX15/0.49 TRIB2/0.49 
MESH:D001064/Appendicitis LPAR4/0.455 MLXIPL/0.454 BSG/0.448 
MESH:D007877/Legionnaires' Disease MLXIPL/0.46 PPARGC1B/0.458 BSG/0.457 
MESH:D004402/Dysautonomia, Familial ACSS2/0.435 MEIS1/0.435 ANGPTL4/0.43 
MESH:D007184/Incontinentia Pigmenti ARF5/0.283 ESRRA/0.283 FKBP4/0.283 
MESH:D055008/Anthracosis PPARGC1B/0.483 MTR/0.483 MLXIPL/0.481 
MESH:D017243/MERRF Syndrome KPNA4/0.44 TNFRSF4/0.44 HSPB8/0.438 
MESH:D005757/Gastritis, Atrophic PPARGC1B/0.484 MTR/0.484 MLXIPL/0.483 
MESH:D053632/X-Linked Combined Immunodeficiency Diseases E2F2/0.329 RBL1/0.329 CCNF/0.329 
MESH:D014380/Tuberculosis, Bovine MLXIPL/0.425 LPAR4/0.422 PPARGC1B/0.418 
MESH:D056731/Donohue Syndrome ARF5/0.292 ESRRA/0.292 FKBP4/0.292 
MESH:D013915/Thrombasthenia E2F2/0.365 RBL1/0.365 CCNF/0.365 
MESH:D018370/Leukocyte-Adhesion Deficiency Syndrome DNAJB11/0.422 LGR5/0.422 SLC39A6/0.422 
MESH:D054098/Thrombocytopenia, Neonatal Alloimmune DNAJB11/0.33 LGR5/0.33 SLC39A6/0.33 
MESH:D016109/Epidermolysis Bullosa, Junctional CGA/0.431 RDH5/0.43 S100A10/0.43 
MESH:D016110/Epidermolysis Bullosa Simplex CGA/0.432 RDH5/0.431 S100A10/0.431 
MESH:D016738/Alagille Syndrome E2F2/0.302 RBL1/0.302 CCNF/0.302 
MESH:D054868/Jacobsen Distal 11q Deletion Syndrome E2F2/0.378 RBL1/0.378 CCNF/0.378 
MESH:D029593/Jervell-Lange Nielsen Syndrome E2F2/0.48 RBL1/0.48 CCNF/0.48 
MESH:D020513/Paralysis, Hyperkalemic Periodic HPRT1/0.366 XRCC1/0.362 DUSP8/0.362 
MESH:D050030/Andersen Syndrome E2F2/0.474 RBL1/0.474 CCNF/0.474 
MESH:D029597/Romano-Ward Syndrome E2F2/0.476 RBL1/0.476 CCNF/0.476 
MESH:D016116/Piebaldism CENPM/0.451 AURKA/0.451 FAM83D/0.451 
MESH:D053546/Keratoderma, Palmoplantar, Epidermolytic RDH5/0.494 CANX/0.49 CCK/0.489 
MESH:D053559/Corneal Dystrophy, Juvenile Epithelial of Meesmann E2F2/0.379 RBL1/0.379 CCNF/0.379 
MESH:D053529/Leukokeratosis, Hereditary Mucosal DNAJB11/0.352 LGR5/0.352 SLC39A6/0.352 
MESH:D053549/Pachyonychia Congenita RDH5/0.389 RETSAT/0.381 S100A10/0.381 
MESH:D062685/Steatocystoma Multiplex RDH5/0.483 RETSAT/0.478 NOG/0.478 
MESH:D053560/Ichthyosis Bullosa of Siemens RDH5/0.358 UBE2C/0.343 PRC1/0.343 
MESH:D018249/Adenoma, Oxyphilic POLK/0.474 DNAJB11/0.474 LGR5/0.474 
MESH:D056734/Monilethrix ARF5/0.32 ESRRA/0.32 FKBP4/0.32 
MESH:D052120/Glycogen Storage Disease Type IIb RAD51AP1/0.371 PPP1R3C/0.368 GTF2H4/0.368 
MESH:D010381/Pelger-Huet Anomaly ARF5/0.323 ESRRA/0.323 FKBP4/0.323 
MESH:D007863/Lecithin Acyltransferase Deficiency GADD45G/0.497 MPEG1/0.497 CENPM/0.496 
MESH:D008557/Melorheostosis TCN2/0.5 SDCBP/0.5 AXIN1/0.5 
MESH:D054877/Wolf-Hirschhorn Syndrome E2F2/0.33 RBL1/0.33 CCNF/0.33 
MESH:D015217/Cholesterol Ester Storage Disease KLK2/0.447 KPNA2/0.447 UBE2C/0.445 
MESH:D008945/Mitral Valve Prolapse PPARGC1B/0.491 TCN2/0.49 AXIN1/0.49 
MESH:D020371/Pelizaeus-Merzbacher Disease ABL1/0.425 ERCC2/0.422 MLH1/0.421 
MESH:D009261/Nail-Patella Syndrome ARF5/0.333 ESRRA/0.333 FKBP4/0.333 
MESH:D018630/Vitreoretinopathy, Proliferative ARF5/0.335 ESRRA/0.335 FKBP4/0.335 
MESH:D002609/Chediak-Higashi Syndrome MLXIPL/0.461 PPARGC1B/0.46 BSG/0.458 
MESH:D008363/alpha-Mannosidosis MVD/0.481 PPP5C/0.48 PRKAR2B/0.48 
MESH:D011504/Protein-Losing Enteropathies SDCBP/0.457 HHIP/0.455 ENO3/0.455 
MESH:D009081/Mucolipidoses HSPB8/0.432 SIK1/0.427 ALAS2/0.427 
MESH:D015408/Gastrinoma ITGAL/0.476 PTEN/0.476 PDK4/0.474 
MESH:D005935/Glucagonoma ITGAL/0.477 PTEN/0.477 PDK4/0.476 
MESH:D018761/Multiple Endocrine Neoplasia Type 1 COX15/0.361 EIF2AK1/0.361 CCDC80/0.361 
MESH:D016115/Albinism, Oculocutaneous MVD/0.42 ITPR1/0.401 PPP5C/0.398 
MESH:D055847/Lynch Syndrome II DNAJB11/0.372 LGR5/0.372 SLC39A6/0.372 
MESH:D055653/Muir-Torre Syndrome CYP2C18/0.398 CHKA/0.395 MT1A/0.395 
MESH:D056587/Cryopyrin-Associated Periodic Syndromes NTM/0.384 DVL2/0.381 SRRD/0.381 
MESH:D018219/Histiocytoma, Benign Fibrous STAT5A/0.5 YBX2/0.499 ITGA3/0.499 
MESH:D054463/Trichothiodystrophy Syndromes ARF5/0.353 ESRRA/0.353 FKBP4/0.353 
MESH:D008556/Melkersson-Rosenthal Syndrome LPAR4/0.392 HOXA11/0.379 PIK3IP1/0.379 
MESH:D009456/Neurofibromatosis 1 SCN4A/0.379 E2F3/0.376 BLVRB/0.376 
MESH:D005126/Eye Burns MLXIPL/0.409 LPAR4/0.404 PPARGC1B/0.402 
MESH:D000012/Abetalipoproteinemia GADD45G/0.499 MPEG1/0.499 PPP5C/0.497 
MESH:D054078/Mevalonate Kinase Deficiency ABL1/0.401 HSPB8/0.398 MT4/0.394 
MESH:D024741/Cardiomyopathy, Hypertrophic, Familial ARF5/0.362 ESRRA/0.362 FKBP4/0.362 
MESH:D052245/Usher Syndromes RBP3/0.491 RBP1/0.491 RDH10/0.491 
MESH:D054364/Solitary Fibrous Tumors COX15/0.493 TRIB2/0.493 EIF2AK1/0.493 
MESH:D055652/Gray Platelet Syndrome ARF5/0.366 ESRRA/0.366 FKBP4/0.366 
MESH:D049932/Nijmegen Breakage Syndrome HHIP/0.457 GLI2/0.457 SUFU/0.457 
MESH:D017253/Neurofibromatoses ARF5/0.369 ESRRA/0.369 FKBP4/0.369 
MESH:D009508/Nevus, Pigmented POLK/0.477 DNAJB11/0.477 LGR5/0.477 
MESH:D016518/Neurofibromatosis 2 SP4/0.437 KCNK4/0.437 SNRNP35/0.437 
MESH:D003635/De Lange Syndrome ARF5/0.374 ESRRA/0.374 FKBP4/0.374 
MESH:D055501/Macrophage Activation Syndrome SDCBP/0.458 HHIP/0.458 GLI2/0.458 
MESH:D006828/Hydatidiform Mole COMTD1/0.478 COX15/0.477 EIF2AK1/0.477 
MESH:D031845/Hajdu-Cheney Syndrome ARF5/0.378 ESRRA/0.378 FKBP4/0.378 
MESH:D046589/CADASIL ACSS2/0.443 MEIS1/0.443 RBP3/0.422 
MESH:D023961/Gonadal Dysgenesis, 46,XX E2F2/0.486 RBL1/0.486 CCNF/0.486 
MESH:D006061/Gonadal Dysgenesis, 46,XY E2F2/0.487 RBL1/0.487 CCNF/0.487 
MESH:D018319/Neurofibrosarcoma BIK/0.476 FDFT1/0.476 AGTR1/0.476 
MESH:D058495/Sotos Syndrome ARF5/0.385 ESRRA/0.385 FKBP4/0.385 
MESH:D015799/Gyrate Atrophy ARF5/0.386 ESRRA/0.386 FKBP4/0.386 
MESH:D009800/Oculocerebrorenal Syndrome ARF5/0.388 ESRRA/0.388 FKBP4/0.388 
MESH:D010040/Otosclerosis DNAJB11/0.424 LGR5/0.424 SLC39A6/0.424 
MESH:D039141/Muscular Dystrophy, Oculopharyngeal RARRES1/0.407 PAX3/0.392 ARF5/0.391 
MESH:D006211/Pantothenate Kinase-Associated Neurodegeneration ARF5/0.392 ESRRA/0.392 FKBP4/0.392 
MESH:D014849/Waardenburg Syndrome DNAJB11/0.455 LGR5/0.455 SLC39A6/0.455 
MESH:D015783/Aniridia ARF5/0.395 ESRRA/0.395 FKBP4/0.395 
MESH:D015324/Pyruvate Carboxylase Deficiency Disease ARF5/0.397 ESRRA/0.397 FKBP4/0.397 
MESH:D014138/Tracheoesophageal Fistula MLXIPL/0.422 LPAR4/0.415 PPARGC1B/0.411 
MESH:D015325/Pyruvate Dehydrogenase Complex Deficiency Disease ARF5/0.399 ESRRA/0.399 FKBP4/0.399 
MESH:D015323/Pyruvate Metabolism, Inborn Errors EZH2/0.453 GNAI3/0.443 ATP6AP1/0.44 
MESH:D056732/Prolidase Deficiency ARF5/0.402 ESRRA/0.402 FKBP4/0.402 
MESH:D052919/Refsum Disease, Infantile TLR8/0.447 MPG/0.447 MLH1/0.447 
MESH:D018902/Chondrodysplasia Punctata, Rhizomelic CD68/0.447 CDC20/0.441 KLK2/0.441 
MESH:D006014/Glycogen Storage Disease Type VII ARF5/0.407 ESRRA/0.407 FKBP4/0.407 
MESH:D062689/Lipoblastoma COX15/0.494 TRIB2/0.494 EIF2AK1/0.494 
MESH:D018877/Sick Building Syndrome ARF5/0.409 ESRRA/0.409 FKBP4/0.409 
MESH:D002549/Diffuse Cerebral Sclerosis of Schilder LPAR4/0.463 ADH1A/0.438 ADH5/0.438 
MESH:D000182/ACTH Syndrome, Ectopic DNAJB11/0.457 LGR5/0.457 SLC39A6/0.457 
MESH:D012207/Rhabdomyoma COX15/0.496 TRIB2/0.496 EIF2AK1/0.496 
MESH:D005489/Focal Dermal Hypoplasia ARF5/0.415 ESRRA/0.415 FKBP4/0.415 
MESH:D004393/Dwarfism, Pituitary LPAR4/0.428 ARF5/0.417 ESRRA/0.417 
MESH:D031901/Gestational Trophoblastic Disease CHST8/0.437 PDK1/0.437 SDC3/0.437 
MESH:D010855/Pierre Robin Syndrome POLE2/0.453 PAWR/0.441 ANGPTL4/0.44 
MESH:D000699/Pain Insensitivity, Congenital ARF5/0.421 ESRRA/0.421 FKBP4/0.421 
MESH:D016098/Gerstmann-Straussler-Scheinker Disease ARF5/0.422 ESRRA/0.422 FKBP4/0.422 
MESH:D034062/Insomnia, Fatal Familial LPAR4/0.471 TTPA/0.461 PRKAA2/0.46 
MESH:D063173/Retrognathia POLE2/0.445 ANGPTL4/0.438 BHLHE40/0.434 
MESH:D008039/Linitis Plastica YBX2/0.5 ITGA3/0.5 COX15/0.5 
MESH:D016715/Proteus Syndrome ARF5/0.428 ESRRA/0.428 FKBP4/0.428 
MESH:D008479/Mediastinal Neoplasms ARF5/0.43 ESRRA/0.43 FKBP4/0.43 
MESH:D015831/Osteochondroma COMTD1/0.477 COX15/0.476 EIF2AK1/0.476 
MESH:D011051/Poliomyelitis ARF5/0.432 ESRRA/0.432 FKBP4/0.432 
MESH:D006013/Glycogen Storage Disease Type VI EZH2/0.493 KIF20A/0.491 CENPM/0.489 
MESH:D011038/Rothmund-Thomson Syndrome ARF5/0.435 ESRRA/0.435 FKBP4/0.435 
MESH:D018813/Multiple Endocrine Neoplasia Type 2a ARF5/0.437 ESRRA/0.437 FKBP4/0.437 
MESH:D018814/Multiple Endocrine Neoplasia Type 2b ARF5/0.438 ESRRA/0.438 FKBP4/0.438 
MESH:D038921/Coffin-Lowry Syndrome RARRES1/0.453 KEAP1/0.45 ACSS2/0.45 
MESH:D041441/Retinoschisis SDCBP/0.46 HHIP/0.46 GLI2/0.46 
MESH:D002973/Cleidocranial Dysplasia ARF5/0.443 ESRRA/0.443 FKBP4/0.443 
MESH:D020512/Myopathy, Central Core LPAR4/0.46 ARF5/0.444 ESRRA/0.444 
MESH:D005497/Follicular Cyst ARF5/0.445 ESRRA/0.445 FKBP4/0.445 
MESH:D010201/Panniculitis, Nodular Nonsuppurative ARF5/0.447 ESRRA/0.447 FKBP4/0.447 
MESH:D058088/Sarcoglycanopathies ARF5/0.448 ESRRA/0.448 FKBP4/0.448 
MESH:D002636/Cherubism ARF5/0.45 ESRRA/0.45 FKBP4/0.45 
MESH:D054312/Buruli Ulcer MLXIPL/0.477 PPARGC1B/0.474 BSG/0.471 
MESH:D053579/Gitelman Syndrome ARF5/0.453 ESRRA/0.453 FKBP4/0.453 
MESH:D015618/Histiocytosis, Sinus PPARGC1B/0.493 TCN2/0.491 AXIN1/0.491 
MESH:D004612/Elliptocytosis, Hereditary ARF5/0.455 ESRRA/0.455 FKBP4/0.455 
MESH:D006250/Hartnup Disease ARF5/0.457 ESRRA/0.457 FKBP4/0.457 
MESH:D055947/Loeys-Dietz Syndrome ARF5/0.458 ESRRA/0.458 FKBP4/0.458 
MESH:D018335/Rhabdoid Tumor ARF5/0.46 ESRRA/0.46 FKBP4/0.46 
MESH:D014897/Spinal Muscular Atrophies of Childhood ARF5/0.461 ESRRA/0.461 FKBP4/0.461 
MESH:D008441/Maxillary Neoplasms ARF5/0.463 ESRRA/0.463 FKBP4/0.463 
MESH:D052536/Niemann-Pick Disease, Type A TRIP13/0.491 CASP14/0.491 RPA3/0.491 
MESH:D052537/Niemann-Pick Disease, Type B TRIP13/0.493 CASP14/0.493 RPA3/0.493 
MESH:D055036/Campomelic Dysplasia ARF5/0.467 ESRRA/0.467 FKBP4/0.467 
MESH:D056770/Netherton Syndrome ARF5/0.468 ESRRA/0.468 FKBP4/0.468 
MESH:D052517/Multiple Sulfatase Deficiency Disease HDAC7/0.496 LMCD1/0.496 TRIP13/0.496 
MESH:D012587/Scimitar Syndrome ARF5/0.471 ESRRA/0.471 FKBP4/0.471 
MESH:D003966/Camurati-Engelmann Syndrome ARF5/0.473 ESRRA/0.473 FKBP4/0.473 
MESH:D006552/Hernia, Inguinal PPARGC1B/0.494 PLTP/0.493 POLE2/0.491 
MESH:D058502/Pentalogy of Cantrell ARF5/0.476 ESRRA/0.476 FKBP4/0.476 
MESH:D004819/Epidermodysplasia Verruciformis ARF5/0.477 ESRRA/0.477 FKBP4/0.477 
MESH:D020288/Papilloma, Choroid Plexus ATP6V1B1/0.5 AVPR2/0.5 RXRG/0.5 
MESH:D013544/Sweat Gland Neoplasms ARF5/0.48 ESRRA/0.48 FKBP4/0.48 
MESH:D020207/Coma, Post-Head Injury ARF5/0.481 ESRRA/0.481 FKBP4/0.481 
MESH:D050336/Mulibrey Nanism ARF5/0.483 ESRRA/0.483 FKBP4/0.483 
MESH:D015826/Langer-Giedion Syndrome PLTP/0.494 TCN2/0.493 POLE2/0.493 
MESH:D003414/Crigler-Najjar Syndrome ARF5/0.486 ESRRA/0.486 FKBP4/0.486 
MESH:D017092/Porphyria, Erythropoietic ARF5/0.487 ESRRA/0.487 FKBP4/0.487 
MESH:D054546/Neuroacanthocytosis ARF5/0.489 ESRRA/0.489 FKBP4/0.489 
MESH:D056725/von Willebrand Disease, Type 1 ARF5/0.49 ESRRA/0.49 FKBP4/0.49 
MESH:D056728/von Willebrand Disease, Type 2 ARF5/0.491 ESRRA/0.491 FKBP4/0.491 
MESH:D056729/von Willebrand Disease, Type 3 ARF5/0.493 ESRRA/0.493 FKBP4/0.493 
MESH:D014923/Wiskott-Aldrich Syndrome ARF5/0.494 ESRRA/0.494 FKBP4/0.494 
MESH:D014929/Wolfram Syndrome ARF5/0.496 ESRRA/0.496 FKBP4/0.496 
MESH:D030321/Denys-Drash Syndrome ARF5/0.497 ESRRA/0.497 FKBP4/0.497 
MESH:D052159/Frasier Syndrome ARF5/0.499 ESRRA/0.499 FKBP4/0.499 
MESH:D030981/Acro-Osteolysis ARF5/0.5 ESRRA/0.5 FKBP4/0.5