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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01351MYPNlarynxMESH:D017114Liver Failure, Acute
HM01351MYPNlarynxMESH:D001321Autistic Disorder
HM01351MYPNlarynxMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM01351MYPNlarynxMESH:D010146Pain
HM01351MYPNlarynxMESH:D000799Angioedemaskin
HM01351MYPNlarynxMESH:D008107Liver Diseasesskin
HM01351MYPNlarynxMESH:D008107Liver Diseasesmuscle
HM01351MYPNlarynxMESH:D008107Liver Diseaseslung
HM01351MYPNlarynxMESH:D008107Liver Diseasesliver
HM01351MYPNlarynxMESH:D006930Hyperalgesia
HM01351MYPNlarynxMESH:D056486Drug-Induced Liver Injury
HM01351MYPNlarynxMESH:D019636Neurodegenerative Diseasesnerve
HM01351MYPNlarynxMESH:D014581Urticariaskin
HM01351MYPNlarynxMESH:D008546Melanoma, Experimental
HM01351MYPNlarynxMESH:D007674Kidney Diseasesureter
HM01351MYPNlarynxMESH:D007674Kidney Diseasespituitary
HM01351MYPNlarynxMESH:D007674Kidney Diseaseskidney
HM01351MYPNlarynxMESH:D002386Cataractpancreas
HM01351MYPNlarynxMESH:D002386Cataracteye