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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01407MESDC2stomachMESH:D007674Kidney Diseasesureter
HM01407MESDC2stomachMESH:D007674Kidney Diseasespituitary
HM01407MESDC2stomachMESH:D007674Kidney Diseaseskidney
HM01407MESDC2stomachMESH:D001321Autistic Disorder
HM01407MESDC2stomachMESH:D011565Psoriasisskin
HM01407MESDC2stomachMESH:D002386Cataractpancreas
HM01407MESDC2stomachMESH:D002386Cataracteye
HM01407MESDC2stomachMESH:D008664Metal Metabolism, Inborn Errorsskin
HM01407MESDC2stomachMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM01407MESDC2stomachMESH:D008664Metal Metabolism, Inborn Errorsliver
HM01407MESDC2stomachMESH:D008664Metal Metabolism, Inborn Errorskidney
HM01407MESDC2stomachMESH:D014985Xerophthalmiaeye
HM01407MESDC2stomachMESH:D056486Drug-Induced Liver Injury
HM01407MESDC2stomachMESH:D009402Nephrosis, Lipoidkidney
HM01407MESDC2stomachMESH:D006930Hyperalgesia
HM01407MESDC2stomachMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM01407MESDC2stomachMESH:D006457Hemoglobinuria, Paroxysmal
HM01407MESDC2stomachMESH:D008546Melanoma, Experimental
HM01407MESDC2stomachMESH:D008107Liver Diseasesskin
HM01407MESDC2stomachMESH:D008107Liver Diseasesmuscle
HM01407MESDC2stomachMESH:D008107Liver Diseaseslung
HM01407MESDC2stomachMESH:D008107Liver Diseasesliver
HM01407MESDC2stomachMESH:D006973Hypertensionlung
HM01407MESDC2stomachMESH:D006973Hypertensionheart
HM01407MESDC2stomachMESH:D006973Hypertensionblood vessel
HM01407MESDC2stomachMESH:D000799Angioedemaskin
HM01407MESDC2stomachMESH:D014581Urticariaskin
HM01407MESDC2stomachMESH:D014605Uveitiseye
HM01407MESDC2stomachMESH:D017114Liver Failure, Acute
HM01407MESDC2stomachMESH:D019636Neurodegenerative Diseasesnerve
HM01407MESDC2stomachMESH:D005355Fibrosis
HM01407MESDC2stomachMESH:D007638Keratoconjunctivitis Siccaeye
HM01407MESDC2stomachMESH:D009404Nephrotic Syndromekidney
HM01407MESDC2stomachMESH:D010146Pain
HM01407MESDC2stomachMESH:D005885Gingival Hyperplasia