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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM03015CD2pharynxMESH:D002386Cataractpancreas
HM03015CD2pharynxMESH:D002386Cataracteye
HM03015CD2pharynxMESH:D001321Autistic Disorder
HM03015CD2pharynxMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM03015CD2pharynxMESH:D017114Liver Failure, Acute
HM03015CD2pharynxMESH:D007333Insulin Resistance
HM03015CD2pharynxMESH:D003110Colonic Neoplasmscolon
HM03015CD2pharynxMESH:D016393Lymphoma, B-Cell
HM03015CD2pharynxMESH:D012130Respiratory Hypersensitivity
HM03015CD2pharynxMESH:D056486Drug-Induced Liver Injury
HM03015CD2pharynxMESH:D013705Temporomandibular Joint Disorders
HM03015CD2pharynxMESH:D008107Liver Diseasesskin
HM03015CD2pharynxMESH:D008107Liver Diseasesmuscle
HM03015CD2pharynxMESH:D008107Liver Diseaseslung
HM03015CD2pharynxMESH:D008107Liver Diseasesliver
HM03015CD2pharynxMESH:D010146Pain
HM03015CD2pharynxMESH:D000799Angioedemaskin
HM03015CD2pharynxMESH:D006930Hyperalgesia
HM03015CD2pharynxMESH:D014581Urticariaskin
HM03015CD2pharynxMESH:D007674Kidney Diseasesureter
HM03015CD2pharynxMESH:D007674Kidney Diseasespituitary
HM03015CD2pharynxMESH:D007674Kidney Diseaseskidney
HM03015CD2pharynxMESH:D019457Chromosome Breakage
HM03015CD2pharynxMESH:D008546Melanoma, Experimental
HM03015CD2pharynxMESH:D007249Inflammation
HM03015CD2pharynxMESH:D019636Neurodegenerative Diseasesnerve
HM03015CD2pharynxMESH:D011471Prostatic Neoplasmsprostate
HM03015CD2pharynxMESH:D001249Asthmalung
HM03015CD2pharynxMESH:D003920Diabetes Mellituspancreas