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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06049LRWD1lymphMESH:D019636Neurodegenerative Diseasesnerve
HM06049LRWD1lymphMESH:D001778Blood Coagulation Disordersbone marrow
HM06049LRWD1lymphMESH:D006930Hyperalgesia
HM06049LRWD1lymphMESH:D055371Acute Lung Injury
HM06049LRWD1lymphMESH:D000799Angioedemaskin
HM06049LRWD1lymphMESH:D056486Drug-Induced Liver Injury
HM06049LRWD1lymphMESH:D009369Neoplasmsspleen
HM06049LRWD1lymphMESH:D009369Neoplasmsbone marrow
HM06049LRWD1lymphMESH:D007333Insulin Resistance
HM06049LRWD1lymphMESH:D017114Liver Failure, Acute
HM06049LRWD1lymphMESH:D007674Kidney Diseasesureter
HM06049LRWD1lymphMESH:D007674Kidney Diseasespituitary
HM06049LRWD1lymphMESH:D007674Kidney Diseaseskidney
HM06049LRWD1lymphMESH:D014581Urticariaskin
HM06049LRWD1lymphMESH:D004487Edema
HM06049LRWD1lymphMESH:D009203Myocardial Infarctionheart
HM06049LRWD1lymphMESH:D003876Dermatitis, Atopicskin
HM06049LRWD1lymphMESH:D008107Liver Diseasesskin
HM06049LRWD1lymphMESH:D008107Liver Diseasesmuscle
HM06049LRWD1lymphMESH:D008107Liver Diseaseslung
HM06049LRWD1lymphMESH:D008107Liver Diseasesliver
HM06049LRWD1lymphMESH:D001321Autistic Disorder
HM06049LRWD1lymphMESH:D008106Liver Cirrhosis, Experimental
HM06049LRWD1lymphMESH:D015427Reperfusion Injury
HM06049LRWD1lymphMESH:D006333Heart Failureheart
HM06049LRWD1lymphMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM06049LRWD1lymphMESH:D015428Myocardial Reperfusion Injury
HM06049LRWD1lymphMESH:D010146Pain
HM06049LRWD1lymphMESH:D006943Hyperglycemia
HM06049LRWD1lymphMESH:D008546Melanoma, Experimental
HM06049LRWD1lymphMESH:D018248Adenoma, Liver Cell
HM06049LRWD1lymphMESH:D008113Liver Neoplasms
HM06049LRWD1lymphMESH:D008113Liver Neoplasms
HM06049LRWD1lymphMESH:D002779Cholestasisliver
HM06049LRWD1lymphMESH:D002386Cataractpancreas
HM06049LRWD1lymphMESH:D002386Cataracteye
HM06049LRWD1lymphMESH:D009765Obesity
HM06049LRWD1lymphMESH:D009135Muscular Diseasesmuscle
HM06049LRWD1lymphMESH:D005234Fatty Liver
HM06049LRWD1lymphMESH:D006529Hepatomegaly