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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06075HMGN4larynxMESH:D008664Metal Metabolism, Inborn Errorsskin
HM06075HMGN4larynxMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM06075HMGN4larynxMESH:D008664Metal Metabolism, Inborn Errorsliver
HM06075HMGN4larynxMESH:D008664Metal Metabolism, Inborn Errorskidney
HM06075HMGN4larynxMESH:D014605Uveitiseye
HM06075HMGN4larynxMESH:D006457Hemoglobinuria, Paroxysmal
HM06075HMGN4larynxMESH:D014985Xerophthalmiaeye
HM06075HMGN4larynxMESH:D006973Hypertensionlung
HM06075HMGN4larynxMESH:D006973Hypertensionheart
HM06075HMGN4larynxMESH:D006973Hypertensionblood vessel
HM06075HMGN4larynxMESH:D009404Nephrotic Syndromekidney
HM06075HMGN4larynxMESH:D011471Prostatic Neoplasmsprostate
HM06075HMGN4larynxMESH:D005355Fibrosis
HM06075HMGN4larynxMESH:D009402Nephrosis, Lipoidkidney
HM06075HMGN4larynxMESH:D007674Kidney Diseasesureter
HM06075HMGN4larynxMESH:D007674Kidney Diseasespituitary
HM06075HMGN4larynxMESH:D007674Kidney Diseaseskidney
HM06075HMGN4larynxMESH:D011565Psoriasisskin
HM06075HMGN4larynxMESH:D005885Gingival Hyperplasia
HM06075HMGN4larynxMESH:D007638Keratoconjunctivitis Siccaeye