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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04841IL20RBpharynxMESH:D014985Xerophthalmiaeye
HM04841IL20RBpharynxMESH:D011565Psoriasisskin
HM04841IL20RBpharynxMESH:D006930Hyperalgesia
HM04841IL20RBpharynxMESH:D002386Cataractpancreas
HM04841IL20RBpharynxMESH:D002386Cataracteye
HM04841IL20RBpharynxMESH:D014605Uveitiseye
HM04841IL20RBpharynxMESH:D009404Nephrotic Syndromekidney
HM04841IL20RBpharynxMESH:D000799Angioedemaskin
HM04841IL20RBpharynxMESH:D006457Hemoglobinuria, Paroxysmal
HM04841IL20RBpharynxMESH:D008546Melanoma, Experimental
HM04841IL20RBpharynxMESH:D009402Nephrosis, Lipoidkidney
HM04841IL20RBpharynxMESH:D007674Kidney Diseasesureter
HM04841IL20RBpharynxMESH:D007674Kidney Diseasespituitary
HM04841IL20RBpharynxMESH:D007674Kidney Diseaseskidney
HM04841IL20RBpharynxMESH:D019636Neurodegenerative Diseasesnerve
HM04841IL20RBpharynxMESH:D006973Hypertensionlung
HM04841IL20RBpharynxMESH:D006973Hypertensionheart
HM04841IL20RBpharynxMESH:D006973Hypertensionblood vessel
HM04841IL20RBpharynxMESH:D008664Metal Metabolism, Inborn Errorsskin
HM04841IL20RBpharynxMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM04841IL20RBpharynxMESH:D008664Metal Metabolism, Inborn Errorsliver
HM04841IL20RBpharynxMESH:D008664Metal Metabolism, Inborn Errorskidney
HM04841IL20RBpharynxMESH:D005355Fibrosis
HM04841IL20RBpharynxMESH:D007638Keratoconjunctivitis Siccaeye
HM04841IL20RBpharynxMESH:D001321Autistic Disorder
HM04841IL20RBpharynxMESH:D014581Urticariaskin
HM04841IL20RBpharynxMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM04841IL20RBpharynxMESH:D008107Liver Diseasesskin
HM04841IL20RBpharynxMESH:D008107Liver Diseasesmuscle
HM04841IL20RBpharynxMESH:D008107Liver Diseaseslung
HM04841IL20RBpharynxMESH:D008107Liver Diseasesliver
HM04841IL20RBpharynxMESH:D005885Gingival Hyperplasia
HM04841IL20RBpharynxMESH:D017114Liver Failure, Acute
HM04841IL20RBpharynxMESH:D056486Drug-Induced Liver Injury
HM04841IL20RBpharynxMESH:D010146Pain