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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05288ZNF697skinMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM05288ZNF697skinMESH:D011565Psoriasisskin
HM05288ZNF697skinMESH:D008664Metal Metabolism, Inborn Errorsskin
HM05288ZNF697skinMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM05288ZNF697skinMESH:D008664Metal Metabolism, Inborn Errorsliver
HM05288ZNF697skinMESH:D008664Metal Metabolism, Inborn Errorskidney
HM05288ZNF697skinMESH:D002294Carcinoma, Squamous Celllung
HM05288ZNF697skinMESH:D002294Carcinoma, Squamous Cellliver
HM05288ZNF697skinMESH:D002294Carcinoma, Squamous Celllarynx
HM05288ZNF697skinMESH:D002294Carcinoma, Squamous Cellkidney
HM05288ZNF697skinMESH:D002294Carcinoma, Squamous Celleye
HM05288ZNF697skinMESH:D007674Kidney Diseasesureter
HM05288ZNF697skinMESH:D007674Kidney Diseasespituitary
HM05288ZNF697skinMESH:D007674Kidney Diseaseskidney
HM05288ZNF697skinMESH:D001943Breast Neoplasmsbreast
HM05288ZNF697skinMESH:D014985Xerophthalmiaeye
HM05288ZNF697skinMESH:D011470Prostatic Hyperplasia
HM05288ZNF697skinMESH:D014605Uveitiseye
HM05288ZNF697skinMESH:D005885Gingival Hyperplasia
HM05288ZNF697skinMESH:D006457Hemoglobinuria, Paroxysmal
HM05288ZNF697skinMESH:D009404Nephrotic Syndromekidney
HM05288ZNF697skinMESH:D005355Fibrosis
HM05288ZNF697skinMESH:D006973Hypertensionlung
HM05288ZNF697skinMESH:D006973Hypertensionheart
HM05288ZNF697skinMESH:D006973Hypertensionblood vessel
HM05288ZNF697skinMESH:D009402Nephrosis, Lipoidkidney
HM05288ZNF697skinMESH:D007638Keratoconjunctivitis Siccaeye
HM05288ZNF697skinMESH:D011471Prostatic Neoplasmsprostate