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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06416TTC1pharynxMESH:D004938Esophageal Neoplasms
HM06416TTC1pharynxMESH:D011565Psoriasisskin
HM06416TTC1pharynxMESH:D005355Fibrosis
HM06416TTC1pharynxMESH:D006973Hypertensionlung
HM06416TTC1pharynxMESH:D006973Hypertensionheart
HM06416TTC1pharynxMESH:D006973Hypertensionblood vessel
HM06416TTC1pharynxMESH:D009395Nephritis, Interstitialkidney
HM06416TTC1pharynxMESH:D009404Nephrotic Syndromekidney
HM06416TTC1pharynxMESH:D005234Fatty Liver
HM06416TTC1pharynxMESH:D005885Gingival Hyperplasia
HM06416TTC1pharynxMESH:D014985Xerophthalmiaeye
HM06416TTC1pharynxMESH:D056486Drug-Induced Liver Injury
HM06416TTC1pharynxMESH:D014605Uveitiseye
HM06416TTC1pharynxMESH:D010391Pemphigoid, Bullousskin
HM06416TTC1pharynxMESH:D007638Keratoconjunctivitis Siccaeye
HM06416TTC1pharynxMESH:D008664Metal Metabolism, Inborn Errorsskin
HM06416TTC1pharynxMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM06416TTC1pharynxMESH:D008664Metal Metabolism, Inborn Errorsliver
HM06416TTC1pharynxMESH:D008664Metal Metabolism, Inborn Errorskidney
HM06416TTC1pharynxMESH:D007674Kidney Diseasesureter
HM06416TTC1pharynxMESH:D007674Kidney Diseasespituitary
HM06416TTC1pharynxMESH:D007674Kidney Diseaseskidney
HM06416TTC1pharynxMESH:D013274Stomach Neoplasms
HM06416TTC1pharynxMESH:D009402Nephrosis, Lipoidkidney
HM06416TTC1pharynxMESH:D006457Hemoglobinuria, Paroxysmal
HM06416TTC1pharynxMESH:D017096Prion Diseasesbrain