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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04107PFN4testisMESH:D000799Angioedemaskin
HM04107PFN4testisMESH:D007638Keratoconjunctivitis Siccaeye
HM04107PFN4testisMESH:D006457Hemoglobinuria, Paroxysmal
HM04107PFN4testisMESH:D009404Nephrotic Syndromekidney
HM04107PFN4testisMESH:D008546Melanoma, Experimental
HM04107PFN4testisMESH:D009402Nephrosis, Lipoidkidney
HM04107PFN4testisMESH:D008107Liver Diseasesskin
HM04107PFN4testisMESH:D008107Liver Diseasesmuscle
HM04107PFN4testisMESH:D008107Liver Diseaseslung
HM04107PFN4testisMESH:D008107Liver Diseasesliver
HM04107PFN4testisMESH:D019636Neurodegenerative Diseasesnerve
HM04107PFN4testisMESH:D001321Autistic Disorder
HM04107PFN4testisMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM04107PFN4testisMESH:D056486Drug-Induced Liver Injury
HM04107PFN4testisMESH:D006930Hyperalgesia
HM04107PFN4testisMESH:D014581Urticariaskin
HM04107PFN4testisMESH:D010146Pain
HM04107PFN4testisMESH:D005355Fibrosis
HM04107PFN4testisMESH:D007674Kidney Diseasesureter
HM04107PFN4testisMESH:D007674Kidney Diseasespituitary
HM04107PFN4testisMESH:D007674Kidney Diseaseskidney
HM04107PFN4testisMESH:D017114Liver Failure, Acute
HM04107PFN4testisMESH:D014985Xerophthalmiaeye
HM04107PFN4testisMESH:D005885Gingival Hyperplasia
HM04107PFN4testisMESH:D008664Metal Metabolism, Inborn Errorsskin
HM04107PFN4testisMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM04107PFN4testisMESH:D008664Metal Metabolism, Inborn Errorsliver
HM04107PFN4testisMESH:D008664Metal Metabolism, Inborn Errorskidney
HM04107PFN4testisMESH:D011565Psoriasisskin
HM04107PFN4testisMESH:D014605Uveitiseye
HM04107PFN4testisMESH:D006973Hypertensionlung
HM04107PFN4testisMESH:D006973Hypertensionheart
HM04107PFN4testisMESH:D006973Hypertensionblood vessel
HM04107PFN4testisMESH:D002386Cataractpancreas
HM04107PFN4testisMESH:D002386Cataracteye