MeSH term	Gene1/score	Gene2/score	Gene3/score	
MESH:D009050/Fluorosis, Dental ENSP00000470770/9.391 FAM25A/8.942 IL13/8.85 
MESH:D001607/Berylliosis CASP3/12.421 IL13RA2/12.104 IL6/11.88 
MESH:D018438/Blue Toe Syndrome NOS2/8.028 VKORC1/7.188 IL10/6.521 
MESH:D006392/Hemangioma, Cavernous IL1B/8.692 NOS2/5.303 CYP3A4/4.03 
MESH:D006971/Hypersplenism TNF/18.584 MAPK1/17.976 IL1B/15.824 
MESH:D055985/Latent Tuberculosis TNF/24.362 CAT/17.974 CXCL8/17.411 
MESH:D012553/Schistosomiasis haematobia TNF/11.375 PRIMA1/9.386 CCDC179/8.41 
MESH:D013322/Strongyloidiasis CXCL8/12.72 IL10/8.682 MAPK3/8.599 
MESH:D015270/Mycobacterium avium-intracellulare Infection NOS2/14.874 CAT/13.116 PTGS2/12.888 
MESH:D013436/Sulfhemoglobinemia RAD51AP2/9.921 C11ORF45/6.072 ENSP00000361463/5.838 
MESH:D038261/Alexander Disease CASP3/8.627 TNF/2.679 IFNG/-6.018 
MESH:D003025/Clubfoot MAPK3/14.912 TP53/10.977 ABCB1/10.894 
MESH:D020936/Epilepsy, Benign Neonatal CASP3/8.627 TNF/2.679 IFNG/-6.018 
MESH:D054066/Leukemia, Large Granular Lymphocytic MAPK1/14.63 MAPK3/12.535 TP53/11.067 
MESH:D009450/Neurodermatitis IL1B/22.086 CYP1A1/19.174 BCL2/17.417 
MESH:D060845/Obsessive Hoarding IL1B/21.968 BCL2/17.366 NOS2/16.258 
MESH:D059348/Peripheral Nerve Injuries ENSP00000358067/10.077 IL6/6.65 MAPK3/6.61 
MESH:D010591/Phantom Limb TNF/25.616 CASP3/22.386 IL6/20.051 
MESH:D020432/Trochlear Nerve Diseases TNF/26.831 CASP3/23.345 IL6/21.024 
MESH:D020295/Brain Stem Neoplasms TNF/12.353 IL6/9.865 IL1B/7.284 
MESH:D003715/Dengue CCL2/11.142 CAT/10.658 PTGS2/10.38 
MESH:D049310/Distal Myopathies TP53/6.433 ALB/5.923 VEGFA/5.72 
MESH:D004240/Diverticulum TNF/-2.385 MAPK1/-15.518 BAX/-15.898 
MESH:D064147/Febrile Neutropenia C19ORF48/10.092 ABCD4/7.841 ABCF3/7.005 
MESH:D005776/Gaucher Disease VKORC1/10.553 APOC4/5.42 ENSP00000321334/5.065 
MESH:D005862/Gerstmann Syndrome TNF/-2.385 MAPK1/-15.432 BAX/-15.804 
MESH:D006491/Hemothorax VKORC1/8.442 ENSP00000437781/8.366 IL10/6.166 
MESH:D006952/Hyperlipoproteinemia Type III SPACA5/15.977 PLGLB1/5.739 ENSP00000321334/5.699 
MESH:D018442/Lymphoma, B-Cell, Marginal Zone CLEC17A/8.929 CFHR2/7.059 MAPK1/6.629 
MESH:D011111/Polymyalgia Rheumatica C19ORF48/11.53 IL1B/7.043 SLC10A2/6.287 
MESH:D011649/Pulmonary Alveolar Proteinosis TNF/13.806 CASP3/10.627 MAPK3/6.879 
MESH:D019082/Smith-Lemli-Opitz Syndrome CASP3/16.252 CCL2/10.26 BAX/10.242 
MESH:D045602/Steatorrhea NOS2/8.639 ENSP00000437781/7.292 CCL2/6.763 
MESH:D002598/Chagas Cardiomyopathy CASP3/16.736 IL6/15.342 IL1B/13.359 
MESH:D000224/Addison Disease HMOX1/9.936 BAX/9.208 CAT/8.636 
MESH:D000849/Anomia NOS2/20.362 CXCL8/19.892 CAT/16.169 
MESH:D001010/Anxiety, Separation TNF/14.003 IL6/9.045 BAX/9.045 
MESH:D020817/Asperger Syndrome TNF/6.163 HTR3B/4.859 ENSP00000347754/4.763 
MESH:D001229/Aspergillosis, Allergic Bronchopulmonary CASP3/29.18 IL6/25.94 NOS2/16.843 
MESH:D002062/Bursitis ENSP00000420093/18.123 TNF/13.057 CXCL8/12.019 
MESH:D002169/Campylobacter Infections KIR3DL3/16.93 ENSP00000383630/15 KIR3DL2/14.474 
MESH:D002279/Carcinoma 256, Walker ENSP00000432622/10.528 C2ORF42/9.847 SMCO3/7.078 
MESH:D002558/Cerebrospinal Fluid Otorrhea CASP3/16.584 IL6/10.805 IL1B/8.217 
MESH:D002559/Cerebrospinal Fluid Rhinorrhea CASP3/16.584 IL6/10.806 IL1B/8.217 
MESH:D041881/Cholecystitis, Acute IL6/10.698 NOS2/10.317 IL1B/7.5 
MESH:D002806/Chondrodysplasia Punctata MAPK1/-9.859 MAPK3/-18.09 BCL2/-18.559 
MESH:D002832/Choroid Hemorrhage MAPK1/-9.859 MAPK3/-18.09 BCL2/-18.559 
MESH:D059350/Chronic Pain CCDC152/9.962 MGAT4A/7.745 FOXL2NB/7.492 
MESH:D003047/Coccidioidomycosis IL6/11.391 IL1B/11.248 MAPK3/7.636 
MESH:D003130/Combat Disorders TNF/14.689 IL6/9.908 BCL2/8.917 
MESH:D046349/Coproporphyria, Hereditary CASP3/17.183 TNF/14.702 MAPK3/13.164 
MESH:D003555/Cystinuria CXCL8/4160272855987006 MAPK1/2605929452521286 C1RL/1928369561979014 
MESH:D019052/Depression, Postpartum PHGR1/8.417 IL6/6.352 IL1B/5.424 
MESH:D004184/Dirofilariasis IL6/16.813 CCL2/10.675 IFNG/10.142 
MESH:D053207/Diurnal Enuresis IL6/10.225 BAX/8.839 IL1B/8.817 
MESH:D004387/Dupuytren Contracture BAX/13.102 CCL2/12.444 HMOX1/11.655 
MESH:D004605/Elephantiasis, Filarial CASP3/19.163 IL1B/15.109 IL6/13.164 
MESH:D004652/Empty Sella Syndrome CASP3/16.584 IL6/10.806 IL1B/8.217 
MESH:D020803/Encephalitis, Herpes Simplex SLC18B1/10.253 IL1B/9.592 NOS2/7.755 
MESH:D017229/Enterobiasis TNF/16.513 CAT/15.659 IL6/12.213 
MESH:D005099/Exotropia IL6/11.108 IL1B/10.574 ENSP00000358067/9.601 
MESH:D005162/Factitious Disorders NOS2/23.099 CXCL8/21.91 CAT/19.282 
MESH:D055111/Failed Back Surgery Syndrome IL6/16.907 FAS/8.483 CASP9/8.349 
MESH:D036981/Fasciitis, Plantar IFNG/9.612 CCL2/9.174 MAPK3/8.873 
MESH:D005329/Fetishism (Psychiatric) FAM71F2/10.554 CYP3A4/10.309 TNF/10.171 
MESH:D005401/Fissure in Ano BAX/13.869 IFNG/12.775 TP53/12.052 
MESH:D006104/Granuloma, Plasma Cell ARMCX2/24.691 GPHA2/8.625 NPVF/7.289 
MESH:D049912/Growth Hormone-Secreting Pituitary Adenoma IL6/15.631 IL1B/12.326 CAT/11.385 
MESH:D006431/Hemobilia MAPK1/-9.859 MAPK3/-18.09 BCL2/-18.559 
MESH:D020065/Hepatopulmonary Syndrome IFNG/3589694897067910 BCL2/3406444596258361 HMOX1/2681627788610827 
MESH:D006712/Homocystinuria ENSP00000432622/8.972 CDPF1/6.672 MMADHC/5.847 
MESH:D006734/Horse Diseases BCL2/10.398 AKT1/5.722 FOS/5.613 
MESH:D006998/Hypochondriasis CXCL8/8.316 UCN2/7.77 CYP3A4/7.3 
MESH:D016114/Ichthyosis, X-Linked IL1B/19.611 CASP3/17.267 CYP3A4/14.325 
MESH:D020299/Intracranial Hemorrhage, Hypertensive BLVRA/9569003704685580 CASP3/8876430930238729 CALCA/7538612797005811 
MESH:D015624/Lambert-Eaton Myasthenic Syndrome TNF/25.633 IL6/15.086 CXCL8/10.986 
MESH:D056929/Liddle Syndrome SMCO3/10.838 NHEDC1/8.491 ENSP00000456039/7.849 
MESH:D008118/Loiasis TNF/22.811 CASP3/20.268 IL1B/14.934 
MESH:D008174/Lung Diseases, Parasitic C19ORF48/9105993649821708 CAT/5075789196095946 MAPK3/4912473041077764 
MESH:D008193/Lyme Disease MAPK1/9.023 MAPK3/8.569 PTGS2/7.568 
MESH:D051359/Lymphohistiocytosis, Hemophagocytic CASP3/10.633 NOS2/9.255 MAPK1/6.848 
MESH:D008230/Lymphomatoid Granulomatosis CASP3/14.732 CYP3A4/10.589 TGFB1/8.754 
MESH:D016779/Malaria, Cerebral MGST2/3843956251180410 TSPO/3408885048695499 FMO1/3090576938753137 
MESH:D016780/Malaria, Vivax MAPK1/6.79 MAPK3/5.31 IL10/4.99 
MESH:D008303/Malignant Carcinoid Syndrome IL6/9.129 BCL2/7.156 MAPK1/5.919 
MESH:D016269/Milk Hypersensitivity SLC43A1/11.065 SPATA25/6.847 IL37/5.703 
MESH:D009084/Mucopolysaccharidosis III TNF/18.706 IL6/13.167 MAPK1/11.11 
MESH:D009471/Neuromyelitis Optica ENSP00000388519/12.736 MAPK3/10.347 IFNG/8.216 
MESH:D020184/Night Terrors IL6/12.658 CAT/9.227 MAPK1/9.21 
MESH:D020189/Nocturnal Myoclonus Syndrome IL6/14.027 TNF/11.597 IL1B/6.593 
MESH:D054318/No-Reflow Phenomenon SMCO3/9.828 ARMCX2/9.164 CXCL8/8.859 
MESH:D009855/Onchocerciasis CASP3/13.423 IL1B/11.071 IL6/10.402 
MESH:D009914/Oral Submucous Fibrosis LYPD5/7.878 MT3/5.731 ENSP00000405610/5.656 
MESH:D016727/Orbital Pseudotumor CCL2/4562992924203755 CCL3/1988369661123306 CYP2C19/1914214481068183 
MESH:D010022/Osteopetrosis ENSP00000388519/24.209 BMF/7.168 PMAIP1/6.853 
MESH:D010123/Oxyuriasis CAT/17.143 TNF/16.533 IL6/12.213 
MESH:D015868/Pars Planitis CASP3/10.633 NOS2/9.255 MAPK1/6.839 
MESH:D010412/Penile Neoplasms CXCL8/13.059 MAPK1/11.591 SLC22A18AS/11.589 
MESH:D047748/Pituitary ACTH Hypersecretion IL6/10.741 TNF/10.524 IL1B/8.493 
MESH:D016066/Pleural Effusion, Malignant SPATA25/8.336 CXCL8/5.517 ATG4D/4.447 
MESH:D011007/Pneumocephalus CASP3/16.584 IL6/10.805 IL1B/8.217 
MESH:D057774/Post-Exercise Hypotension NOS2/23.099 CXCL8/21.91 CAT/19.282 
MESH:D011218/Prader-Willi Syndrome TNF/14.689 IL6/9.91 BCL2/8.919 
MESH:D053448/Prostatism IL6/13.742 TNF/11.885 PTGS2/8.709 
MESH:D011475/Prosthesis Failure IL6/20.561 CYP3A4/15.557 CCL2/11.689 
MESH:D055732/Pulmonary Aspergillosis MAPK3/14.277 ENSP00000388519/12.483 CCL2/12.124 
MESH:D020425/Radial Neuropathy CYP4F3/3040593454063030 ENSP00000331831/2010219165258610 MTHFR/1921733229557024 
MESH:D053120/Respiratory Aspiration CHRNB3/8.205 CXCL8/7.612 CHRNA9/5.972 
MESH:D012214/Rheumatic Heart Disease MGST2/8484097344579458 UBC/8234493958252149 PLB1/5617278027933833 
MESH:D045169/Severe Acute Respiratory Syndrome ENSP00000388519/9.756 MAPK3/9.053 CCL2/8.171 
MESH:D020922/Sleep-Wake Transition Disorders SMCO3/10.801 CXCL8/9.779 CCL2/6.598 
MESH:D012913/Snoring ENSP00000469960/8.054 TTYH2/7.548 CLIC3/7.037 
MESH:D013130/Spinal Stenosis CASP3/9.383 CXCL8/8.283 NOS2/6.196 
MESH:D013174/Sporotrichosis CASP3/29.18 IL6/26.048 NOS2/16.843 
MESH:D013319/Strongyle Infections, Equine IL6/11.883 BAX/8.606 BCL2/7.244 
MESH:D052879/Subacute Combined Degeneration UBC/2257571614723576 RELA/1416726512310799 PARP1/920724739091648 
MESH:D050798/SUNCT Syndrome C2ORF42/9.253 ARMCX2/5.989 ENSP00000383630/5.786 
MESH:D013742/Tetanus IL1B/14.245 CYP1A2/9.127 IFNG/9.098 
MESH:D014008/Tinea Pedis IL6/20.324 IL1B/17.119 IFNG/14.699 
MESH:D015845/Tonic Pupil GSTO2/12287332974524178 TMEM266/9743791925692486 PLA2G12A/8355888793676181 
MESH:D014125/Toxoplasmosis, Congenital CASP3/10.633 NOS2/9.255 MAPK1/6.808 
MESH:D014126/Toxoplasmosis, Ocular CASP3/9.028 NOS2/6.814 MAPK1/5.934 
MESH:D014135/Tracheal Stenosis CASP3/20.685 CYP3A4/15.215 CYP2D6/11.955 
MESH:D014235/Trichinellosis ENSP00000396505/12.255 SMCO3/7.221 ARMCX2/6.681 
MESH:D014252/Trichostrongyloidiasis BCL2/16.532 CCL2/14.055 VEGFA/11.962 
MESH:D014353/Trypanosomiasis, African IL6/18.545 IL1B/13.63 CXCL8/12.77 
MESH:D014437/Typhus, Endemic Flea-Borne AKT1/2029999071242287 CYP1A1/1453201541754660 CASP9/1399228372290499 
MESH:D001748/Urinary Bladder Neck Obstruction TNF/15.64 IL6/6.913 IFNG/6.447 
MESH:D014627/Vaginitis CAT/11.885 MAPK3/11.751 PTGS2/11.309 
MESH:D014802/Vitamin A Deficiency SDR9C7/9.223 RDH16/7.745 IL6/7.6 
MESH:D000196/Actinomycosis SLC51B/27.822 IL6/13.118 CYP3A4/12.879 
MESH:D000347/Afibrinogenemia IL1B/6.101 NOS2/3.587 CYP3A4/2.058 
MESH:D016263/AIDS-Associated Nephropathy CCDC160/27.252 BMT2/6.589 SMCO2/5.633 
MESH:D053714/Aspermia C2ORF42/22.39 SLC51A/15.545 TDRD10/9.191 
MESH:D001250/Asthma, Exercise-Induced TP53/8.984 ABCB1/8.593 TGFB1/7.855 
MESH:D016863/Bacillaceae Infections NOS2/3736988210086623 TP53/3073612012068894 SLC22A2/2140460598770412 
MESH:D001437/Bacteriuria MAPK1/13.466 BCL2/12.192 MAPK3/11.911 
MESH:D002915/Chylous Ascites IFNG/466655840006008 NFE2L2/381230228657110 IL6/9.486 
MESH:D044903/Congenital Hyperinsulinism ABCB1/10.179 CAT/9.524 IFNG/8.956 
MESH:D003665/Decompression Sickness IL10/9.846 HMOX1/9.153 IL13RA2/9.008 
MESH:D012628/Dermatitis, Seborrheic IL6/12.469 IL1B/10.754 BCL2/8.651 
MESH:D004454/Echolalia BAX/20.307 IFNG/20.089 MAPK3/19.541 
MESH:D004653/Empyema TNF/24.372 IL6/17.696 CYP3A4/16.337 
MESH:D004749/Entamoebiasis TNF/30.167 CASP3/21.333 CXCL8/16.33 
MESH:D005335/Fever of Unknown Origin LILRB1/10.624 IL6/8.957 IL1B/8.022 
MESH:D016469/Fungemia IL6/11.523 IL1B/10.732 CXCL8/9.578 
MESH:D006506/Hepatitis A CCL2/7.355 CXCL8/6.808 BAX/6.74 
MESH:D007647/Kernicterus C2ORF50/10.947 FAM200A/7.278 SPANXA2/4.833 
MESH:D017513/Lichen Nitidus C9ORF153/17516868510328634 METTL9/14392229569151532 FXYD4/8580874313901908 
MESH:D034701/Mastocytosis, Cutaneous ENSP00000456039/8.965 CASP3/6.493 PTGER4/6.03 
MESH:D010677/Philadelphia Chromosome SLC51B/20.389 TMEM200C/5.927 CCDC146/5.72 
MESH:D011001/Pleuropneumonia PSORS1C2/22503242746805020 SLCO4A1/9748949386532166 SLC17A3/8295590182673664 
MESH:D013530/Surgical Wound Infection NOS2/11.033 PTGS2/9.463 SLC51A/8.899 
MESH:D013945/Thymoma AKT1/1837091851841929 CYP1A2/1471409320670215 IL12B/1464947330010631 
MESH:D018382/Thyroid Hormone Resistance Syndrome TNF/9.994 ENSP00000443070/8.84 IL6/6.468 
MESH:D016862/Tuberculoma, Intracranial MAPK1/9.447 ABCB1/9.187 CAT/9.179 
MESH:D053202/Urinary Incontinence, Urge DEFB4A/12.409 CASP3/11.118 CYP3A4/8.875 
MESH:D004204/Dislocations TNF/17.342 CASP3/15.284 LILRA6/14.412 
MESH:D004834/Epilepsy, Post-Traumatic VCY/12.683 MT4/10.462 VWC2L/7.244 
MESH:D010483/Periapical Diseases ENSP00000409197/10.701 ENSP00000314807/7 CCRL2/6.749 
MESH:D046351/Protoporphyria, Erythropoietic IL6/21.861 IL1B/20.919 CXCL8/18.841 
MESH:D012223/Rhinitis, Vasomotor CASP3/12.255 IL6/11.347 CYP3A4/11.252 
MESH:D004238/Diverticulitis IL13/8.144 TPMT/7.621 SLC51A/6.429 
MESH:D001063/Appendiceal Neoplasms TNF/16.88 CASP3/13.09 IL6/11.203 
MESH:D018409/Foot Injuries TNF/15.649 CASP3/13.341 CYP3A4/11.772 
MESH:D054882/Antley-Bixler Syndrome Phenotype TNF/12.93 CYP1A1/10.797 CASP3/10.166 
MESH:D002179/Candidiasis, Cutaneous TNF/12.823 CYP1A1/11.072 CASP3/10.711 
MESH:D020152/Antithrombin III Deficiency IL1B/6.101 NOS2/3.587 CYP3A4/2.058 
MESH:D003440/Croup ABCB1/20.821 IFNG/19.759 CXCL8/19.129 
MESH:D005596/Fractures, Closed IFNG/10.606 BAX/10.504 IL13RA2/9.118 
MESH:D016489/Head Injuries, Closed NAAA/5.927 NAPEPLD/4.817 VEGFD/4.753 
MESH:D007925/Leriche Syndrome IL1B/6.101 NOS2/3.587 CYP3A4/2.058 
MESH:D020221/Optic Nerve Injuries NOXA1/16.363 DDIAS/11.755 MT4/11.131 
MESH:D011186/Postphlebitic Syndrome IL1B/5.508 NOS2/3.162 CYP3A4/2.124 
MESH:D019315/Retrobulbar Hemorrhage IL1B/5.643 NOS2/3.73 IFNG/3.112 
MESH:D020206/Subarachnoid Hemorrhage, Traumatic IL1B/6.101 NOS2/3.587 CYP3A4/2.058 
MESH:D014847/Vulvitis CYP3A4/13.612 TNF/11.159 IL6/9.763 
MESH:D000275/Adjustment Disorders TNF/27.796 IL6/22.732 MAPK3/16.834 
MESH:D000881/Anthrax NOS2/14.333 PTGS2/12.709 CCL2/12.669 
MESH:D001442/Bacteroides Infections SLC51A/22.534 TNF/10.702 IL6/9.459 
MESH:D057215/Body Dysmorphic Disorders TNF/30.164 IL6/23.679 BAX/18.052 
MESH:D002371/Cat Diseases CXCL8/8.657 CYP1A1/6.899 BCL2/6.076 
MESH:D014355/Chagas Disease CASP3/12.909 IL1B/10.595 CYP3A4/9.556 
MESH:D003874/Dermatitis Herpetiformis CASP3/32.345 TNF/31.559 IL6/26.364 
MESH:D004404/Dysentery, Amebic TNF/10.929 IL1B/8.854 TSNAXIP1/8.793 
MESH:D005873/Giardiasis IL6/16.222 IL1B/15.677 BAX/12.283 
MESH:D016460/Granuloma Annulare CASP3/32.467 TNF/31.559 IL6/26.364 
MESH:D006981/Hyperthyroxinemia MT3/6.764 TSGA13/4.869 IL6/4.362 
MESH:D009494/Neurosyphilis CASP3/20.708 IL10/15.89 CYP3A4/13.726 
MESH:D010000/Osteitis CAT/12.931 NOS2/11.062 PTGS2/9.902 
MESH:D010241/Parakeratosis C2ORF50/18.076 ENSP00000431049/12.923 CYP2S1/11.899 
MESH:D046350/Porphyria, Variegate TNF/19.717 CASP3/17.795 ENSP00000382318/12.174 
MESH:D014245/Trichomonas Infections TNF/19.741 CASP3/16.522 IL6/15.807 
MESH:D014247/Trichomonas Vaginitis TNF/19.727 CASP3/16.084 IL6/15.896 
MESH:D014435/Typhoid Fever SLC51A/10.484 NOS2/9.125 ALB/8.619 
MESH:D053584/Urinoma ENSP00000388519/21.391 ENSP00000396505/15.394 TNFSF12/8.851 
MESH:D004405/Dysentery, Bacillary CASP3/26.668 IL6/25.653 MAPK1/18.967 
MESH:D001885/Bordetella Infections IL6/-2.015 CASP3/-11.024 IFNG/-13.36 
MESH:D020165/Carbamoyl-Phosphate Synthase I Deficiency Disease MT4/12.109 TEX43/11.409 VKORC1/7.547 
MESH:D057973/Dent Disease CALCRL/13.146 LILRB1/12.243 NOXA1/12.095 
MESH:D045826/Flavobacteriaceae Infections IL6/-2.015 CASP3/-11.024 IFNG/-13.36 
MESH:D005926/Glossalgia ENSP00000383630/16.463 KIR3DL3/13.211 TNF/11.584 
MESH:D006958/Hyperostosis, Cortical, Congenital SPATA32/717705435.492 SUMO2/353079933.532 UTY/327140985.931 
MESH:D018783/Impotence, Vasculogenic BCL2/10.608 CXCL8/8.969 IFNG/8.943 
MESH:D006008/Glycogen Storage Disease IL1B/8.157 UCN3/6.989 CYP3A4/6.144 
MESH:D055092/Laryngomalacia IL1B/10.778 CYP3A4/6.183 CCL2/5.864 
MESH:D046768/Nesidioblastosis IL1B/10.778 CYP3A4/6.183 MAPK3/5.352 
MESH:D006393/Hemangiopericytoma ERICH3/11.425 PRR9/7.905 XK/6.471 
MESH:D007636/Keratoacanthoma SPATA25/5.473 IL6/5.469 NOS2/3.831 
MESH:D015211/Zellweger Syndrome CASP3/3280140353694823 CYSLTR2/2473651173431453 ALOX12/2079304901863496 
MESH:D006563/Herpes Zoster Ophthalmicus ACMSD/3359212269501388 AFMID/2895143909811376 ENSP00000407952/1118570129268870 
MESH:D016697/Herpes Zoster Oticus AFMID/2895143909025304 ENSP00000407952/1118570128706100 HLA-DOA/745810878105849 
MESH:D009377/Multiple Endocrine Neoplasia ABCB1/6.049 MGST2/5.944 UGT1A8/5.873 
MESH:D015882/Retinal Necrosis Syndrome, Acute CASP3/20.504 BAX/17.161 IL6/16.691 
MESH:D019121/Burkholderia Infections IL1B/14.798 BAX/10.098 BCL2/8.932 
MESH:D002916/Chylothorax IL1B/14.766 BAX/10.23 ENSP00000469538/8.893 
MESH:D012035/Refsum Disease ENSP00000469538/13.93 MGLL/6.651 IL1B/6.334 
MESH:D002472/Cell Transformation, Viral UBALD2/10.704 FAM25A/10.594 FAM25E/10.123 
MESH:D001162/Arteriosclerosis Obliterans BLVRA/9.486 TNF/6.7 CXCL8/6.024 
MESH:D020330/Bell Palsy NOS2/15.076 BCL2/14.131 CAT/13.943 
MESH:D005627/Frostbite CYP3A4/19.371 MAPK1/19.152 BAX/17.392 
MESH:D006484/Hemorrhoids BAX/19.55 MAPK3/19.477 MAPK1/18.794 
MESH:D001469/Barotrauma NOS2/16.531 BCL2/14.914 BAX/14.72 
MESH:D002647/Chilblains TNF/10.666 CASP3/8.135 IL1B/5.689 
MESH:D005142/Eyelid Neoplasms MAPK1/16.516 IL6/15.842 IFNG/14.665 
MESH:D005928/Glossitis TNF/16.934 CASP3/13.024 IL6/10.465 
MESH:D006012/Glycogen Storage Disease Type V NPPC/4220806972904768 TSTD2/3214543727597372 CASP3/2495466487435808 
MESH:D046089/Hearing Loss, Mixed Conductive-Sensorineural IL1B/21.125 MAPK1/14.451 BAX/14.278 
MESH:D020243/Infarction, Anterior Cerebral Artery CASP3/11.097 TNF/10.666 IL1B/5.659 
MESH:D017574/Parasystole IL1B/21.461 MAPK1/15.136 BAX/14.892 
MESH:D011000/Pleurodynia, Epidemic IL6/10.149 NOXA1/10.116 IL1B/8.257 
MESH:D011017/Pneumonia, Lipid TNF/6176986275111473 NOS2/2842532193098766 CYP1A1/2544845258798741 
MESH:D011024/Pneumonia, Viral CYP3A4/-13.475 NOS2/-13.919 CCL2/-16.276 
MESH:D011027/Pneumoperitoneum CASP3/12.076 TNF/10.666 IL1B/5.661 
MESH:D013991/Tietze's Syndrome TNF/31.091 CASP3/18.367 MAPK1/17.294 
MESH:D058267/Flea Infestations CYP3A4/11.125 CXCL8/9.48 MAPK1/9.038 
MESH:D006725/Hookworm Infections MAPK1/15.885 MAPK3/15.553 BCL2/13.22 
MESH:D006925/Hymenolepiasis PTGS2/9.27 ABCB1/9.016 IL10/8.73 
MESH:D017194/Oxyurida Infections BCL2/14.351 CCL2/13.519 VEGFA/8.641 
MESH:D013984/Tick Infestations IL1F7/286.055 C5ORF60/218.923 SMIM10/210.62 
MESH:D014257/Trichuriasis CYP3A4/11.271 CYP1A1/9.305 CXCL8/8.911 
MESH:D001404/Babesiosis FAM175A/110420776.815 CCRL2/78798726.611 PLA2G4D/60725180.87 
MESH:D010520/Aggressive Periodontitis CXCL8/11.748 BCL2/11.727 BAX/11.587 
MESH:D015161/Dementia, Multi-Infarct BCL2/11.719 BAX/11.587 CXCL8/11.393 
MESH:D015155/Esophageal Spasm, Diffuse IFNG/-11.605 NOS2/-11.925 BCHE/-13.253 
MESH:D046649/Hematoma, Subdural, Spinal CXCL8/16.753 ABCB1/16.157 CYP1A1/16.039 
MESH:D015576/Hyperostosis IL1B/9.928 IL10/9.513 BAX/8.89 
MESH:D007589/Job Syndrome CXCL8/12.312 BCL2/11.73 BAX/11.587 
MESH:D029503/Anemia, Diamond-Blackfan C2ORF42/13.745 SMCO3/9.347 CYBRD1/8.136 
MESH:D011645/Puerperal Infection SPATA25/15.074 TNF/12.012 ENSP00000469960/10.685 
MESH:D005878/Gilbert Disease TEX44/13.479 ENSP00000467123/9.01 FABP12/7.272 
MESH:D004382/Duodenitis ENSP00000388519/14.299 IFNG/7.817 TP53/7.751 
MESH:D010864/Pilonidal Sinus ENSP00000388519/15.952 NOS2/12.642 BCL2/11.814 
MESH:D003784/Dental Pulp Calcification ENSP00000470580/10.492 ENSP00000470478/10.097 CYP2R1/8.985 
MESH:D000026/Abortion, Habitual LRRC75A/9.355 SPATA25/8.752 TNXB/7.869 
MESH:D004604/Elephantiasis ENSP00000469538/23.203 TMEM255A/19.47 TM6SF2/16.361 
MESH:D054989/Nephrogenic Fibrosing Dermopathy IL13RA2/9.774 ACKR4/9.43 ENSP00000456039/7.294 
MESH:D059265/Visceral Pain NAT9/9.137 SALL4/8.981 DPPA3/8.701 
MESH:D002430/Cecal Neoplasms TNF/10.583 CASP3/10.289 IL6/7.174 
MESH:D007046/Hysteria IL6/10.997 IL1B/9.682 BCL2/7.316 
MESH:D058540/Aicardi Syndrome NPPC/4231124451112650 PRL/3127393281282852 CASP3/2495466693927568 
MESH:D009347/Nelson Syndrome TNF/4816709266482891 CASP3/4479170244148130 CYP3A4/4201936464107939 
MESH:D001238/Asphyxia Neonatorum SMCO3/12.098 ENSP00000469669/5.819 CNP/4.92 
MESH:D004444/Echinococcosis, Hepatic CASP3/20.229 IL6/14.851 NOS2/14.045 
MESH:D020211/Autonomic Dysreflexia ENSP00000296847/17.427 BCL2/16.866 IL6/14.02 
MESH:D005146/Facial Asymmetry ENSP00000296847/22.079 BCL2/14.993 IL6/14.96 
MESH:D057891/Tetraploidy ENSP00000296847/15.983 SAMD3/10.89 CENPX/10.856 
MESH:D000751/Anemia, Neonatal SYNC/9969701350059066 ENSP00000296847/5313428583582978 CXCL8/4129312346738522 
MESH:D056735/Autoimmune Lymphoproliferative Syndrome CXCL8/8.683 IL1B/7.82 MAPK1/7.109 
MESH:D010623/Phencyclidine Abuse IL1B/5.108 FMO4/5.033 IL6/4.895 
MESH:D012791/Shy-Drager Syndrome TMIE/7258291574453402 CISD2/4746632412972540 ENSP00000367360/4180919025375244 
MESH:D014190/Transvestism TNF/8.256 IL6/7.698 UBC/7.377 
MESH:D005536/Foot-and-Mouth Disease FAS/6.606 TGFB1/6.419 CYP3A4/6.32 
MESH:D006337/Heart Murmurs TAS2R46/2760190742742856 SLC22A2/2139700763638615 CASP3/2071698125870500 
MESH:D046648/Hematoma, Subdural, Intracranial ATP6AP1L/16.806 ARMCX1/13.053 ENSP00000420093/12.021 
MESH:D006939/Hyperemesis Gravidarum NPVF/13.758 CASP3/12.079 CYP3A4/11.337 
MESH:D054243/Vesicular Stomatitis CYP3A4/7.057 FAS/6.953 VEGFA/5.657 
MESH:D020235/Gait Apraxia IL6/6147400085496925 IL10/3295435099179761 FOS/2182998842299970 
MESH:D057066/Low Tension Glaucoma ENSP00000456039/13977785624414768 SAT2/6617301594815712 CASP3/6237358554584548 
MESH:D018235/Smooth Muscle Tumor IL6/3547259980784006 SPATA31A3/2105156183391557 CYP3A4/1851580218449676 
MESH:D007228/Infant Nutrition Disorders IL1B/3776427572045042 PTGS2/1550392634299881 CAT/1459527710192088 
MESH:D007815/Larva Migrans PTGS2/1571105691835206 CAT/1467312417372225 CCL3/527307609088262 
MESH:D013031/Sparganosis IL1B/3302494750576302 PTGS2/1578894877065713 CAT/1454187730887177 
MESH:D006009/Glycogen Storage Disease Type II C19ORF38/28.12 CASP3/19.942 TNF/16.089 
MESH:D010309/Parotitis UBC/5500807251505857 TP53/5008188291223280 TNF/4493195838146888 
MESH:D017695/Soft Tissue Injuries BLVRA/8.295 CES2/6.813 CYP3A4/6.594 
MESH:D003291/Conversion Disorder CASP3/38.864 CYP3A4/26.332 IL1B/25.79 
MESH:D005955/Glucosephosphate Dehydrogenase Deficiency BAX/8.161 CCL2/5.981 PTGS2/4.094 
MESH:D006395/Hemarthrosis BAX/8.16 CCL2/5.981 PTGS2/4.095 
MESH:D006478/Hemorrhagic Fever, American CYP3A4/-10.684 NOS2/-11.599 BCL2/-14.463 
MESH:D006479/Hemorrhagic Fever, Crimean CYP3A4/-10.684 NOS2/-13.338 BCL2/-14.463 
MESH:D006480/Hemorrhagic Fever with Renal Syndrome NOS2/-11.599 BAX/-12.669 CYP3A4/-13.562 
MESH:D058437/Hypertensive Retinopathy NOS2/8.28 CXCL8/7.197 CYP3A4/7.076 
MESH:D020192/Lafora Disease BAX/8.16 CCL2/5.981 PTGS2/4.095 
MESH:D007835/Lassa Fever CYP3A4/-12.483 NOS2/-13.338 CASP9/-16.154 
MESH:D020720/Myasthenia Gravis, Autoimmune, Experimental KIR3DL3/6740817856918885 FAM157A/3897340364403743 PTGS2/2928972898492952 
MESH:D018184/Paramyxoviridae Infections CYP3A4/-10.684 NOS2/-11.599 BCL2/-14.463 
MESH:D010217/Phlebotomus Fever CYP3A4/-9.292 BCL2/-11.08 NOS2/-11.599 
MESH:D012088/Reoviridae Infections NOS2/-11.599 CYP3A4/-12.483 BAX/-15.442 
MESH:D012295/Rift Valley Fever CYP3A4/-10.949 NOS2/-11.599 BCL2/-15.441 
MESH:D017565/Sarcoidosis, Pulmonary NOS2/-11.599 CYP3A4/-12.483 CCL2/-16.366 
MESH:D013344/Subacute Sclerosing Panencephalitis NOS2/-11.599 CYP3A4/-12.483 BAX/-15.449 
MESH:D006960/Hyperoxaluria, Primary NOXA1/15.981 TNF/10.793 HEG1/10.367 
MESH:D005222/Mental Fatigue CCDC149/8516408648804492 CASP3/5005458766604937 TIPARP/3474915001433114 
MESH:D056693/Propionic Acidemia LAMTOR5/8952277092156447 CAMK2N2/8752165938413765 UBC/7992913812102519 
MESH:D016869/Ureaplasma Infections CAT/13.295 CYP1A1/13.244 MAPK3/12.886 
MESH:D014901/West Nile Fever MAPK1/10.748 MAPK3/10.153 CAT/9.827 
MESH:D049913/ACTH-Secreting Pituitary Adenoma TNF/4831202741768543 CASP3/4466078879499902 CYP3A4/4181810650111936 
MESH:D007827/Laryngitis ABCB1/15.312 CYP3A4/15.02 BAX/13.354 
MESH:D000033/Abortion, Threatened CASP3/12.556 CEP95/12.551 ENSP00000420093/11.824 
MESH:D012488/Salpingitis TNF/13.667 CXCL8/12.732 MAPK1/10.311 
MESH:D004169/Diphyllobothriasis CAT/15.939 CASP3/14.456 PTGS2/14.429 
MESH:D005585/Influenza in Birds IL12B/10.405 PELI3/8.077 IL37/7.436 
MESH:D010378/Pedophilia TMIE/23.898 GPHA2/22.283 LILRA6/21.94 
MESH:D012222/Rhinitis, Atrophic DEPTOR/15.653 PRR5L/15.406 IL1B/12.552 
MESH:D005258/Felty Syndrome CYP2D6/-14.845 CASR/-18.66 MPO/-19.595 
MESH:D049950/Hyperparathyroidism, Primary UBC/11641099813786536 ENSP00000470770/8009368097920876 TSPO/5241637623263852 
MESH:D056650/Vulvodynia C2ORF42/53.063 SPATA25/10.553 SH3TC2/9.608 
MESH:D001899/Borrelia Infections MAPK1/9.023 MAPK3/8.569 PTGS2/7.568 
MESH:D015456/Leukemia, Biphenotypic, Acute SPATA25/12.41 NR2C2AP/7.506 ENSP00000469799/6.987 
MESH:D020852/Lyme Neuroborreliosis FGD6/5432701110954851 TTC23/4828347274286913 IL6/4601993730336089 
MESH:D001261/Pulmonary Atelectasis ENSP00000469046/5.663 DDIAS/5.36 IL33/5.201 
MESH:D013202/Staphylococcal Food Poisoning UBC/8.652 IL33/6.135 ACKR2/5.97 
MESH:D056833/Central Serous Chorioretinopathy TNF/25.165 IL1B/18.528 IL4/18.298 
MESH:D019557/Dermatitis, Perioral CASP3/11.38 IL1B/10.052 CXCL8/9.387 
MESH:D005357/Fibrous Dysplasia of Bone MAPK3/1670788276002066 NOS2/1329345863152655 TGFB1/890673916451747 
MESH:D004881/Ergotism TAS2R20/51.621 TAS2R30/49.282 ENSP00000472293/11.729 
MESH:D014136/Tracheitis LTB/8.717 CASP3/6.832 CCL2/5.957 
MESH:D000274/Adiposis Dolorosa IL1B/29.45 NOS2/17.477 PTGS2/15.126 
MESH:D017789/Granuloma, Pyogenic ENSP00000396505/23.032 CAT/15.491 RAD51AP2/14.124 
MESH:D018327/Hutchinson's Melanotic Freckle ENSP00000396505/23.496 IL2/10.959 CYP3A4/10.814 
MESH:D045822/Intestinal Volvulus CASP3/3998118019112751 CYP3A4/3132608984381022 TNF/3064232745556057 
MESH:D058387/Candidemia IL6/7.808 IL1B/7.244 CYP3A4/4.932 
MESH:D003112/Colonic Pseudo-Obstruction IL6/14.883 MAPK3/11.381 MCRIP2/9.571 
MESH:D007762/Labyrinthitis IL6/9.184 IL1B/9.092 CYP3A4/5.665 
MESH:D009091/Mucormycosis IL1B/10.008 IL6/7.749 CYP3A4/7.082 
MESH:D020096/Zygomycosis IL6/7.751 LILRB1/7.297 CYP3A4/7.082 
MESH:D015823/Acanthamoeba Keratitis FMO1/8800908780258223 FAM175A/7602689543312942 ENSP00000441269/7552076893909684 
MESH:D004842/Epispadias CSHL1/2073061360792990 CYP3A4/1792222204854482 CASP3/1788598154078776 
MESH:D015787/Erythema Chronicum Migrans GTF3C1/9091431978131072 EIF2D/9060910979946166 NEU4/8617127665063360 
MESH:D007169/Impetigo CAT/1987170606919139 NOS2/1879039962977866 PTGS2/1156735337246061 
MESH:D011539/Pruritus Vulvae POU2F3/4926639766916725 GAL3ST1/3713591694924233 PNLDC1/3644005883317271 
MESH:D013896/Thoracic Diseases C17ORF82/-11.001 CASP3/-11.915 REN/-13.328 
MESH:D016643/Encephalopathy, Bovine Spongiform CASP3/17.139 TNF/16.776 MAPK3/14.297 
MESH:D055964/Alien Hand Syndrome BASP1/11168968471647070 GGCX/4047528848607078 CYP2A6/2875611596870220 
MESH:D002825/Chorioretinitis TNF/9337393148194994 TPMT/7067064035741928 IL1B/5335257782645269 
MESH:D061219/Olfactory Nerve Injuries SPATA25/25913307912153172 IL1F7/17725648157173482 ZC3H12A/15529610556996960 
MESH:D010214/Papillon-Lefevre Disease SPATA25/8916313722119972 TNF/5928286546550758 BID/4135809877937527 
MESH:D011694/Purpura, Hyperglobulinemic CASP3/8.625 IL6/8.565 IL1B/7.843 
MESH:D010246/Paralysis, Obstetric CCDC179/13.237 CEP112/-4.402 SLC22A2/-7.311 
MESH:D013547/Sweating, Gustatory TNF/-11.963 KCNH2/-13.292 CASP3/-14.314 
MESH:D001478/Basal Cell Nevus Syndrome REG1B/26.842 TUSC2/15.609 DISP2/13.022 
MESH:D004619/Embolism, Amniotic Fluid NOXA1/18.216 IGFL4/13.44 C1QL2/12.011 
MESH:D054331/Sertoli Cell-Only Syndrome ENSP00000345684/11039539629760430 SPATA25/10661894728145750 BANP/5722246116393979 
MESH:D008336/Mandibular Diseases COL28A1/28.175 LOXL4/20.438 COL20A1/19.4 
MESH:D054084/Myocardial Bridging IL6/4662471468048240 TNF/3737113195197862 MAPK3/3442907733102296 
MESH:D004684/Leukoencephalitis, Acute Hemorrhagic TNF/22.041 CXCL8/17.823 CYP3A4/14.385 
MESH:D013180/Sprains and Strains TNF/81.803 IL6/49.74 IL1B/18.864 
MESH:D003410/Cri-du-Chat Syndrome UBC/8712414977600871 TNF/5931919522579161 CASP3/4877007968878821 
MESH:D053578/Opsoclonus-Myoclonus Syndrome TNF/6608921734070719 CASP3/5748311364784215 IL1B/4266653039824956 
MESH:D029241/Optic Atrophy, Autosomal Dominant TNF/34.932 NOS2/14.955 CASP3/12.607 
MESH:D014391/Tuberculosis, Miliary CYP3A4/3387142189862762 BCL2/2155962454491312 MAPK3/1721581379478158 
MESH:D020786/Hemangioma, Cavernous, Central Nervous System IL1B/6.101 NOS2/3.587 CYP3A4/2.058 
MESH:D011666/Pulmonary Valve Stenosis ELAVL1/7714334839736732 TNF/6866562132149282 PRDM10/6753910739670118 
MESH:D019142/Hemorrhagic Fever, Ebola UBC/3.061 ZFAND4/2.54 POTEF/2.452 
MESH:D008457/Measles NOS2/-11.599 CYP3A4/-12.483 CCL2/-15.96 
MESH:D011855/Radiodermatitis SPATA32/10.044 GMCL1/6.5 CYP3A4/4.089 
MESH:D015518/Rett Syndrome ALB/7090960639087182 TP53/6826972275253855 MYC/6015694124008681 
MESH:D011535/Prune Belly Syndrome CYP3A4/-4.353 CASP3/-11.527 TNF/-13.109 
MESH:D010013/Osteogenesis Imperfecta MAPK3/1569942385777436 NOS2/1239034711834116 TGFB1/895058341468778 
MESH:D058926/Intraoperative Awareness ALB/2767529021241272 SLC22A2/2726928566858916 CASP8/2307615946420824 
MESH:D015012/Yersinia pseudotuberculosis Infections CASP3/0.147 BCL2/-9.228 CYP3A4/-11.053 
MESH:D003963/Diaper Rash TNF/-6.054 IL6/-9.158 CASP3/-9.331 
MESH:D054061/Ischemic Contracture TNF/6191969224082088 CASP3/4627202630269861 IL6/4470117302069439 
MESH:D056824/Upper Extremity Deep Vein Thrombosis CYP3A4/4420282938673632 F3/2762820426552851 PROCR/2381358485319524 
MESH:D055744/Invasive Pulmonary Aspergillosis MGST1/10964404302422974 FMO3/10828075846448314 FMO2/10136674824104472 
MESH:D020953/Neuroaspergillosis FMO1/13430646741557292 GSTA5/12949304148477218 AP1AR/12585860411320252 
MESH:D010229/Paracoccidioidomycosis ALOX12/8050650944500892 TPMT/6724795026109916 GSTM2/6102230411909387 
MESH:D058734/Exsanguination IL6/-12.4 TNF/-15.378 CYP2C8/-15.926 
MESH:D013716/Tennis Elbow F8A1/44837428463013096 LGALS13/38352434016063840 BEST4/19014462168643248 
MESH:D002581/Uterine Cervical Incompetence GPHA2/19.54 LRRC75A/17.138 CSHL1/13.576 
MESH:D016585/Vaginosis, Bacterial IL6/16545507388095280 ABCB1/16424759728012062 CASP3/15983455143536160 
MESH:D018658/Ventricular Septal Rupture F8A1/39755704292941256 LGALS13/34200764721743400 BEST4/16935959068350566 
MESH:D015419/Spastic Paraplegia, Hereditary TNF/13.806 CASP3/10.63 MAPK3/6.879 
MESH:D002812/Chondroma UBC/-19.186 SPATA32/-21.49 ELAVL1/-21.58 
MESH:D004416/Dysplastic Nevus Syndrome PRDX3/-18.639 CAT/-19.432 MAPK1/-19.451 
MESH:D004403/Dysentery IL6/13.121 CXCL8/11.485 OBP2A/10.148 
MESH:D011604/Psychoses, Alcoholic CASP3/-3.763 DRD3/-10.015 CYP3A4/-10.059 
MESH:D055112/Pyometra TNF/-6.273 NOS2/-7.813 CASP3/-9.643 
MESH:D006053/Goldenhar Syndrome CASP3/-19.772 AKT1/-19.847 TNF/-20.402 
MESH:D028226/Amyloidosis, Familial CES2/7644335631735878 UGT1A9/3840112935527517 AKT1/3436630751978150 
MESH:D002275/Carcinoid Heart Disease PSPN/32.928 HYAL4/19.119 GFRA4/19.079 
MESH:D028227/Amyloid Neuropathies, Familial CYP1A2/4962400455030516 CYP1A1/4570541735312782 CES2/3626580964210135 
MESH:D010585/Phagocyte Bactericidal Dysfunction BAX/11.587 BCL2/11.531 CXCL8/10.946 
MESH:D004774/Entropion GABRB2/0.541 CYP3A4/-5.293 POMC/-11.808 
MESH:D005693/Galactosemias ALB/6719958640633975 CTNNB1/5472765734918172 BCL2/5454179122636360 
MESH:D000795/Fabry Disease UBC/3.692 ELAVL1/1.659 POTEF/0.915 
MESH:D015163/Superinfection ENSP00000383672/43235761523476488 HLA-DQA2/18781114996817816 CLEC2B/14924386670772304 
MESH:D018215/Osteoblastoma ENSP00000364702/77.25 CASP3/1.124 NAT2/-4.767 
MESH:D010157/Palatal Neoplasms UBC/38.566 TSPO/2.864 SLC6A8/-4.743 
MESH:D043204/Mineralocorticoid Excess Syndrome, Apparent BAX/12.876 BCL2/12.501 CAT/11.439 
MESH:D007718/Knee Injuries TSPO/3093950412376973 TP53/1992025255398122 CXCL8/1691877966490186 
MESH:D010007/Osteochondritis TSPO/3093950412376973 TP53/1992025255605566 CXCL8/1691877966918332 
MESH:D000793/Angioid Streaks CYP3A4/-14.17 BAX/-15.477 ABCB1/-15.497 
MESH:D007625/Kearns-Sayre Syndrome CASP3/10.633 NOS2/9.255 MAPK1/6.844 
MESH:D013161/Splenic Rupture RELA/-10.386 BAX/-12.732 CASP3/-13.493 
MESH:D000189/Actinobacillus Infections MMP2/-12.078 CASP3/-16.212 TNF/-16.309 
MESH:D005674/Fusobacterium Infections MMP2/-12.078 CASP3/-16.212 TNF/-16.309 
MESH:D009506/Nevus PRDX3/-18.639 CAT/-19.432 MAPK1/-19.451 
MESH:D000052/Acanthosis Nigricans TNF/-14.49 CCL2/-14.866 GH1/-15.594 
MESH:D006616/Hip Contracture CES1/-15.885 CES2/-16.397 DRD2/-19.307 
MESH:D055013/Osteoarthritis, Spine CES1/-15.885 CES2/-16.397 DRD2/-19.307 
MESH:D012783/Shoulder Dislocation CES1/-15.885 CES2/-16.397 DRD2/-19.307 
MESH:D054082/Lissencephaly PLAT/2742855397168804 APLP2/2713501012412792 CP/2523156688863134 
MESH:D008342/Mandibulofacial Dysostosis CASP3/-19.772 AKT1/-19.847 TNF/-20.402 
MESH:D002239/Carbohydrate Metabolism, Inborn Errors PTGS2/6.479 MAPK1/5.487 ABCB1/4.848 
MESH:D017282/Tick-Borne Diseases MAPK1/11.938 MAPK3/11.26 PTGS2/11.013 
MESH:D010032/Otitis Externa TNF/160.939 SLC22A2/27.38 NFKBIA/6.903 
MESH:D008587/Meningitis, Viral IL6/-8.46 CASP3/-9.666 IL1B/-9.967 
MESH:D013478/Superior Mesenteric Artery Syndrome PNLDC1/16063231008751960 UBC/14186553122587610 RSC1A1/12405911647558570 
MESH:D001117/Arenaviridae Infections NOS2/-13.338 CYP3A4/-13.562 CCL2/-15.322 
MESH:D052858/Cystocele NPPB/2984386847032651 GADD45A/2823281800142800 CYP2D6/1982898687694353 
MESH:C535803/succinic semialdehyde dehydrogenase deficiency CASP3/4.648 TNF/4.127 IL6/2.199 
MESH:C535506/Episodic Ataxia, Type 2 TNF/10.612 IL6/0.856 IL1B/-0.954 
MESH:C564777/Male Germ Cell Tumor TNF/22.515 IL6/19.373 MAPK1/15.381 
MESH:C537345/Sitosterolemia CASP3/6.679 IL1B/6.3 CYP3A4/5.787 
MESH:C536871/Spastic paraplegia type 5A, recessive TNF/19.181 CASP3/15.644 CYP3A4/9.785 
MESH:C536915/Thyroid cancer, papillary C19ORF48/9.346 SLC51B/6.798 IL6/6.712 
MESH:C535804/Stargardt disease 1 SDR9C7/17.381 PNPLA4/14.587 RDH8/12.973 
MESH:C535438/Bidirectional tachycardia IL10/8.704 CYP1A1/8.619 PTGS2/8.434 
MESH:C536010/Achalasia microcephaly TNF/4900826849134861 C19ORF48/3971291705508829 IL6/2697059185397922 
MESH:C538481/Acquired CJD SPATA31E1/2740.188 SPANXN3/2740.188 ENSP00000366731/2740.188 
MESH:C565662/Acth-Independent Macronodular Adrenal Hyperplasia IL10/21.627 CAT/17.578 BCL2/16.92 
MESH:C562942/Aortic Valve, Calcification of MAPK1/2.699 MAPK3/2.337 BCL2/2.261 
MESH:C537422/Apparent mineralocorticoid excess BAX/16.591 BCL2/15.924 CAT/13.698 
MESH:C538045/Chromosome 17 deletion CASP3/20.225 IFNG/13.24 CYP3A4/13.01 
MESH:C535323/Chromosome 5q Deletion Syndrome CASP3/12.072 CYP3A4/11.511 IFNG/9.925 
MESH:C537814/Chromosome 7, monosomy CASP3/20.225 IFNG/13.236 CYP3A4/13.15 
MESH:C538499/Erythema migrans, lingual CAT/17.236 MAPK1/11.735 MAPK3/10.793 
MESH:C538556/Imerslund-Grasbeck syndrome CASP3/28.329 IL1B/24.753 ENSP00000432622/21.956 
MESH:C536312/Juvenile pauciarticular chronic arthritis CASP3/8.095 CXCL8/7.641 CYP3A4/7.009 
MESH:C540770/Mitochondrial cytopathy CASP3/10.106 NOS2/7.932 MAPK1/6.993 
MESH:C537072/Nonpuerperal galactorrhea CASP3/18.719 IL6/11.947 IL1B/7.823 
MESH:C537884/Peters anomaly MAPK1/2.699 MAPK3/2.337 BCL2/2.261 
MESH:C536683/Warfarin syndrome MAPK1/2.699 MAPK3/2.337 BCL2/2.261 
MESH:C536855/Fanconi like syndrome BCL2/9.494 BAX/8.707 IL10/8.326 
MESH:C535838/Pancreatic islet cell tumors IL6/13.518 CYP3A4/8.706 NOS2/7.708 
MESH:C538446/Speech disturbance - use of faulty phrasing and unrelated words HMOX1/4842053170925878 PTGS2/4595114946643633 TH/1910825268746724 
MESH:C562730/Adenocarcinoma Of Esophagus NT5C1B/17418701676146832 NT5C3A/13180581403058464 NT5M/12348025474272136 
MESH:C536610/Familial cerebral cavernous malformation IL1B/6.182 NOS2/3.397 CYP3A4/2.311 
MESH:C537156/Hypoparathyroidism familial isolated SLC51B/34.819 FABP6/8.746 C19ORF48/7.119 
MESH:C537150/Hypoglycemia, leucine-induced IL1B/15.458 CYP3A4/9.07 MAPK1/8.6 
MESH:C538543/Preeclamptic toxemia IL1B/15.434 MAPK1/9.605 CYP3A4/9.07 
MESH:C537480/Miyoshi myopathy ARMCX2/15.596 KIAA0408/11.992 BAX/8.295 
MESH:C536957/Temporomandibular ankylosis TNF/10945867092553970 IL37/6266481548707108 CXCL8/5637691656273000 
MESH:C531755/Kidney disorder involving deposition of calcium and oxalate or phosphate in the renal tubules IL1B/15.368 BAX/12.481 NOS2/11.411 
MESH:C536773/Syphilis, secondary TNF/9853901547875096 IFNG/6664637260493298 CASP3/5857450082213060 
MESH:C536380/Evans Syndrome CXCL8/7.371 MAPK3/4.589 VEGFA/4.271 
MESH:C538457/Segmental glomerulosclerosis FAM25A/9.166 TAS2R20/9.081 TAS2R30/9.081 
MESH:C535485/Chromosome 13q trisomy CXCL8/13.345 CYP1A1/13.091 PTGS2/12.555 
MESH:C548016/Hypermanganesemia with Dystonia Polycythemia and Cirrhosis ENSP00000437781/35.706 MT4/18.486 TXNRD3NB/11.975 
MESH:C536409/Neural tube defect, folate-sensitive ENSP00000422293/11.027 IL6/9.936 CASP3/9.554 
MESH:C537358/Methylmalonic acidemia NDUFA4/4615650439802084 COX7A1/3978492586521464 CD320/3866696983378077 
MESH:C538007/Dystonia, Dopa-responsive TNF/13.608 IL6/8.122 CYP3A4/7.372 
MESH:C538421/Neurodegeneration with brain iron accumulation (NBIA) TNF/13.608 IL6/8.122 CYP3A4/7.372 
MESH:C537537/Segawa syndrome, autosomal recessive IL6/3738336809432836 NOS2/2681531052511168 NRGN/1896210107640018 
MESH:C536330/Polycystic liver disease TP53TG3/14.533 ENSP00000358599/11.819 SPATA31A3/9.184 
MESH:C536901/Thrombotic thrombocytopenic purpura, acquired BAX/8.054 CCL2/6.777 CYP3A4/5.688 
MESH:C538110/Pancreatic adenoma GPHA2/17.497 SMCO3/17.157 CYP3A4/8.337 
MESH:C535953/Eosinophilic pustular folliculitis CYP3A4/16.949 CAT/15.872 CYP1A1/15.084 
MESH:C537055/Alopecia universalis TNF/23.101 IL1B/15.707 IL6/10.808 
MESH:C537748/Omphalocele exstrophy imperforate anus TNF/19.551 IL6/11.329 CASP3/11.195 
MESH:C538117/Human Herpesvirus 6 encephalitis ANKAR/10420898092984294 CASP3/7900419686666326 SLC34A1/5382963894693755 
MESH:C531609/Diffuse alopecia CYP2D6/-11.882 CASR/-15.281 MPO/-19.459 
MESH:C562477/Halothane Hepatitis CASP3/10.929 CXCL8/9.739 CAT/6.443 
MESH:C536063/Osteoporosis-pseudoglioma syndrome IL1B/19.714 BAX/15.809 MAPK3/14.343 
MESH:C538542/Sexual precocity BAX/1698022077376808 IL10/621429619738618 CYP1A1/505080085137311 
MESH:C536561/Trimethylaminuria PLGLB1/14.003 C14ORF80/12.725 P3H4/10.748 
MESH:C562393/Melanoma, Cutaneous Malignant ELAVL1/14496302181828666 PRDM10/12419975031943386 UBC/11430165925126548 
MESH:C537658/Basal ganglia disease, biotin-responsive CASP3/12538624144333644 CXCL8/10203364276427398 MAPK3/9667233937161044 
MESH:C538169/Acitretin embryopathy BID/6752199044849799 TNF/5741227839282235 CRADD/3458654149874080 
MESH:C537417/Butyrylcholinesterase deficiency HYKK/13157208262575926 RIC3/8620813241071421 CHRNA9/7209530901730538 
MESH:C536783/T-Lymphocytopenia BIRC8/9.613 TP53TG3/9.157 UBC/7.141 
MESH:C535563/Absence of Tibia ABCB1/11222662325340082 CYP2D6/5675617394642678 BAX/5603936442430328 
MESH:C565891/Calcification of Joints and Arteries MAGEB17/27705788910788408 MEPE/17102028934471362 MAGEE2/16018273215330218 
MESH:C535598/Creatine deficiency, X-linked ENSP00000332389/9217231170969778 IL1B/4969338499032990 TP53/3155554277771888 
MESH:C536694/Westphal disease TNF/5771791149287786 MAPK1/3812303533792375 IL6/3103787454440204 
MESH:C564013/Deafness, Aminoglycoside-Induced TNF/14.144 CASP3/13.768 IL6/11.488 
OMIM:248310/PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL TNF/7084361719745706 CASP3/6410414677244683 IL1B/4895568868192826 
MESH:C535469/Coproporphyria CES4A/14363752132338168 CLEC14A/12313514794163432 WFDC2/8563559608122820 
MESH:C537700/Juvenile osteoporosis CASP3/8.334 ADA/-11.671 SOD1/-13.082 
MESH:C535306/2-Hydroxyglutaricaciduria UBC/-18.539 SPATA32/-20.748 ELAVL1/-20.753 
MESH:C537630/Birdshot chorioretinopathy CYP3A4/-10.248 CYP2C9/-12.326 ABCB1/-12.844 
MESH:C537880/Lathosterolosis CYP4F2/3751543843623718 SPATA32/3600141416465215 SREBF1/3540439025693833