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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05983C21orf119heartMESH:D006973Hypertensionlung
HM05983C21orf119heartMESH:D006973Hypertensionheart
HM05983C21orf119heartMESH:D006973Hypertensionblood vessel
HM05983C21orf119heartMESH:D011565Psoriasisskin
HM05983C21orf119heartMESH:D007674Kidney Diseasesureter
HM05983C21orf119heartMESH:D007674Kidney Diseasespituitary
HM05983C21orf119heartMESH:D007674Kidney Diseaseskidney
HM05983C21orf119heartMESH:D006457Hemoglobinuria, Paroxysmal
HM05983C21orf119heartMESH:D014985Xerophthalmiaeye
HM05983C21orf119heartMESH:D009404Nephrotic Syndromekidney
HM05983C21orf119heartMESH:D007638Keratoconjunctivitis Siccaeye
HM05983C21orf119heartMESH:D005885Gingival Hyperplasia
HM05983C21orf119heartMESH:D005355Fibrosis
HM05983C21orf119heartMESH:D014605Uveitiseye
HM05983C21orf119heartMESH:D008664Metal Metabolism, Inborn Errorsskin
HM05983C21orf119heartMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM05983C21orf119heartMESH:D008664Metal Metabolism, Inborn Errorsliver
HM05983C21orf119heartMESH:D008664Metal Metabolism, Inborn Errorskidney
HM05983C21orf119heartMESH:D009402Nephrosis, Lipoidkidney