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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06091ARXpancreasMESH:D000799Angioedemaskin
HM06091ARXpancreasMESH:D056486Drug-Induced Liver Injury
HM06091ARXpancreasOMIM:300215LISSENCEPHALY, X-LINKED, 2
HM06091ARXpancreasMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM06091ARXpancreasOMIM:300004CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA
HM06091ARXpancreasMESH:D014581Urticariaskin
HM06091ARXpancreasMESH:D007674Kidney Diseasesureter
HM06091ARXpancreasMESH:D007674Kidney Diseasespituitary
HM06091ARXpancreasMESH:D007674Kidney Diseaseskidney
HM06091ARXpancreasMESH:D019636Neurodegenerative Diseasesnerve
HM06091ARXpancreasMESH:C536300Partington X-linked mental retardation syndrome
HM06091ARXpancreasMESH:D002386Cataractpancreas
HM06091ARXpancreasMESH:D002386Cataracteye
HM06091ARXpancreasMESH:D008107Liver Diseasesskin
HM06091ARXpancreasMESH:D008107Liver Diseasesmuscle
HM06091ARXpancreasMESH:D008107Liver Diseaseslung
HM06091ARXpancreasMESH:D008107Liver Diseasesliver
HM06091ARXpancreasMESH:D038901Mental Retardation, X-Linked
HM06091ARXpancreasMESH:D008546Melanoma, Experimental
HM06091ARXpancreasMESH:D001321Autistic Disorder
HM06091ARXpancreasOMIM:308350EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1
HM06091ARXpancreasMESH:D010146Pain
HM06091ARXpancreasMESH:D017114Liver Failure, Acute
HM06091ARXpancreasMESH:D006930Hyperalgesia