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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06565FAM161AeyeMESH:D019636Neurodegenerative Diseasesnerve
HM06565FAM161AeyeMESH:D006930Hyperalgesia
HM06565FAM161AeyeMESH:D000799Angioedemaskin
HM06565FAM161AeyeMESH:D009402Nephrosis, Lipoidkidney
HM06565FAM161AeyeMESH:D006973Hypertensionlung
HM06565FAM161AeyeMESH:D006973Hypertensionheart
HM06565FAM161AeyeMESH:D006973Hypertensionblood vessel
HM06565FAM161AeyeMESH:D014581Urticariaskin
HM06565FAM161AeyeMESH:D014605Uveitiseye
HM06565FAM161AeyeMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM06565FAM161AeyeMESH:D056486Drug-Induced Liver Injury
HM06565FAM161AeyeMESH:D006457Hemoglobinuria, Paroxysmal
HM06565FAM161AeyeMESH:D008546Melanoma, Experimental
HM06565FAM161AeyeMESH:D008664Metal Metabolism, Inborn Errorsskin
HM06565FAM161AeyeMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM06565FAM161AeyeMESH:D008664Metal Metabolism, Inborn Errorsliver
HM06565FAM161AeyeMESH:D008664Metal Metabolism, Inborn Errorskidney
HM06565FAM161AeyeMESH:D011565Psoriasisskin
HM06565FAM161AeyeMESH:D007638Keratoconjunctivitis Siccaeye
HM06565FAM161AeyeMESH:D008107Liver Diseasesskin
HM06565FAM161AeyeMESH:D008107Liver Diseasesmuscle
HM06565FAM161AeyeMESH:D008107Liver Diseaseslung
HM06565FAM161AeyeMESH:D008107Liver Diseasesliver
HM06565FAM161AeyeMESH:D009404Nephrotic Syndromekidney
HM06565FAM161AeyeMESH:D010146Pain
HM06565FAM161AeyeMESH:D014985Xerophthalmiaeye
HM06565FAM161AeyeMESH:D017114Liver Failure, Acute
HM06565FAM161AeyeMESH:D001321Autistic Disorder
HM06565FAM161AeyeMESH:D007674Kidney Diseasesureter
HM06565FAM161AeyeMESH:D007674Kidney Diseasespituitary
HM06565FAM161AeyeMESH:D007674Kidney Diseaseskidney
HM06565FAM161AeyeMESH:D002386Cataractpancreas
HM06565FAM161AeyeMESH:D002386Cataracteye
HM06565FAM161AeyeMESH:D005885Gingival Hyperplasia
HM06565FAM161AeyeMESH:D005355Fibrosis
HM06565FAM161AeyeMESH:D012174Retinitis Pigmentosamuscle