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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06112FPGTtracheaMESH:D011565Psoriasisskin
HM06112FPGTtracheaMESH:D006973Hypertensionlung
HM06112FPGTtracheaMESH:D006973Hypertensionheart
HM06112FPGTtracheaMESH:D006973Hypertensionblood vessel
HM06112FPGTtracheaMESH:D008664Metal Metabolism, Inborn Errorsskin
HM06112FPGTtracheaMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM06112FPGTtracheaMESH:D008664Metal Metabolism, Inborn Errorsliver
HM06112FPGTtracheaMESH:D008664Metal Metabolism, Inborn Errorskidney
HM06112FPGTtracheaMESH:D010523Peripheral Nervous System Diseasesnerve
HM06112FPGTtracheaMESH:D015658HIV Infections
HM06112FPGTtracheaMESH:D014605Uveitiseye
HM06112FPGTtracheaMESH:D014985Xerophthalmiaeye
HM06112FPGTtracheaMESH:D009374Neoplasms, Experimental
HM06112FPGTtracheaMESH:D004362Drug Toxicity
HM06112FPGTtracheaMESH:D005355Fibrosis
HM06112FPGTtracheaMESH:D009404Nephrotic Syndromekidney
HM06112FPGTtracheaMESH:D009437Neuralgia
HM06112FPGTtracheaMESH:D007638Keratoconjunctivitis Siccaeye
HM06112FPGTtracheaMESH:D006457Hemoglobinuria, Paroxysmal
HM06112FPGTtracheaMESH:D005234Fatty Liver
HM06112FPGTtracheaMESH:D009202Cardiomyopathies
HM06112FPGTtracheaMESH:D009402Nephrosis, Lipoidkidney
HM06112FPGTtracheaMESH:D007674Kidney Diseasesureter
HM06112FPGTtracheaMESH:D007674Kidney Diseasespituitary
HM06112FPGTtracheaMESH:D007674Kidney Diseaseskidney
HM06112FPGTtracheaMESH:D005885Gingival Hyperplasia
HM06112FPGTtracheaMESH:D008223Lymphoma