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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06228FEM1CtracheaMESH:D006457Hemoglobinuria, Paroxysmal
HM06228FEM1CtracheaMESH:D005355Fibrosis
HM06228FEM1CtracheaMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM06228FEM1CtracheaMESH:D007674Kidney Diseasesureter
HM06228FEM1CtracheaMESH:D007674Kidney Diseasespituitary
HM06228FEM1CtracheaMESH:D007674Kidney Diseaseskidney
HM06228FEM1CtracheaMESH:D011565Psoriasisskin
HM06228FEM1CtracheaMESH:D014605Uveitiseye
HM06228FEM1CtracheaMESH:D006930Hyperalgesia
HM06228FEM1CtracheaMESH:D009404Nephrotic Syndromekidney
HM06228FEM1CtracheaMESH:D002386Cataractpancreas
HM06228FEM1CtracheaMESH:D002386Cataracteye
HM06228FEM1CtracheaMESH:D008664Metal Metabolism, Inborn Errorsskin
HM06228FEM1CtracheaMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM06228FEM1CtracheaMESH:D008664Metal Metabolism, Inborn Errorsliver
HM06228FEM1CtracheaMESH:D008664Metal Metabolism, Inborn Errorskidney
HM06228FEM1CtracheaMESH:D008546Melanoma, Experimental
HM06228FEM1CtracheaMESH:D014581Urticariaskin
HM06228FEM1CtracheaMESH:D010146Pain
HM06228FEM1CtracheaMESH:D056486Drug-Induced Liver Injury
HM06228FEM1CtracheaMESH:D019636Neurodegenerative Diseasesnerve
HM06228FEM1CtracheaMESH:D014985Xerophthalmiaeye
HM06228FEM1CtracheaMESH:D017114Liver Failure, Acute
HM06228FEM1CtracheaMESH:D005885Gingival Hyperplasia
HM06228FEM1CtracheaMESH:D000799Angioedemaskin
HM06228FEM1CtracheaMESH:D001321Autistic Disorder
HM06228FEM1CtracheaMESH:D008107Liver Diseasesskin
HM06228FEM1CtracheaMESH:D008107Liver Diseasesmuscle
HM06228FEM1CtracheaMESH:D008107Liver Diseaseslung
HM06228FEM1CtracheaMESH:D008107Liver Diseasesliver
HM06228FEM1CtracheaMESH:D006973Hypertensionlung
HM06228FEM1CtracheaMESH:D006973Hypertensionheart
HM06228FEM1CtracheaMESH:D006973Hypertensionblood vessel
HM06228FEM1CtracheaMESH:D009402Nephrosis, Lipoidkidney
HM06228FEM1CtracheaMESH:D007638Keratoconjunctivitis Siccaeye