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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06909UGT2B28prostateMESH:D005076Exanthemaskin
HM06909UGT2B28prostateOMIM:607208DRAVET SYNDROME
HM06909UGT2B28prostateMESH:D011297Prenatal Exposure Delayed Effects
HM06909UGT2B28prostateMESH:D004362Drug Toxicity
HM06909UGT2B28prostateMESH:D017029Epilepsy, Complex Partialmuscle
HM06909UGT2B28prostateMESH:D004831Epilepsies, Myoclonicmuscle
HM06909UGT2B28prostateMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM06909UGT2B28prostateMESH:D004916Erythromelalgiablood vessel
HM06909UGT2B28prostateMESH:D012893Sleep Disorders
HM06909UGT2B28prostateMESH:D019310Pseudolymphoma
HM06909UGT2B28prostateMESH:D004816Epidermal Necrolysis, Toxic
HM06909UGT2B28prostateMESH:D006965Hyperplasia
HM06909UGT2B28prostateMESH:D019465Craniofacial Abnormalities
HM06909UGT2B28prostateMESH:D004342Drug Hypersensitivity
HM06909UGT2B28prostateMESH:D008180Lupus Erythematosus, Systemicbone marrow
HM06909UGT2B28prostateMESH:D004827Epilepsymuscle
HM06909UGT2B28prostateMESH:D010018Osteomalaciabone
HM06909UGT2B28prostateMESH:D010146Pain
HM06909UGT2B28prostateOMIM:167400PAROXYSMAL EXTREME PAIN DISORDER
HM06909UGT2B28prostateMESH:D011248Pregnancy Complications
HM06909UGT2B28prostateMESH:D009224Myotonia Congenitanerve
HM06909UGT2B28prostateMESH:D012640Seizuresmuscle
HM06909UGT2B28prostateMESH:D013262Stevens-Johnson Syndromeskin
HM06909UGT2B28prostateMESH:D020138Hyperhomocysteinemia
HM06909UGT2B28prostateMESH:D004828Epilepsies, Partialmuscle
HM06909UGT2B28prostateMESH:D056486Drug-Induced Liver Injury
HM06909UGT2B28prostateMESH:D009421Nervous System Malformations
HM06909UGT2B28prostateMESH:D008607Mental Retardation
HM06909UGT2B28prostateMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM06909UGT2B28prostateMESH:D000014Abnormalities, Drug-Induced
HM06909UGT2B28prostateMESH:D001714Bipolar Disorder
HM06909UGT2B28prostateMESH:D010267Parapsoriasisskin