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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06466PIGNtracheaMESH:D009404Nephrotic Syndromekidney
HM06466PIGNtracheaMESH:D012878Skin Neoplasms
HM06466PIGNtracheaMESH:D008664Metal Metabolism, Inborn Errorsskin
HM06466PIGNtracheaMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM06466PIGNtracheaMESH:D008664Metal Metabolism, Inborn Errorsliver
HM06466PIGNtracheaMESH:D008664Metal Metabolism, Inborn Errorskidney
HM06466PIGNtracheaMESH:D014985Xerophthalmiaeye
HM06466PIGNtracheaMESH:D014605Uveitiseye
HM06466PIGNtracheaMESH:D006457Hemoglobinuria, Paroxysmal
HM06466PIGNtracheaMESH:D006973Hypertensionlung
HM06466PIGNtracheaMESH:D006973Hypertensionheart
HM06466PIGNtracheaMESH:D006973Hypertensionblood vessel
HM06466PIGNtracheaMESH:D007674Kidney Diseasesureter
HM06466PIGNtracheaMESH:D007674Kidney Diseasespituitary
HM06466PIGNtracheaMESH:D007674Kidney Diseaseskidney
HM06466PIGNtracheaMESH:D011565Psoriasisskin
HM06466PIGNtracheaMESH:D009402Nephrosis, Lipoidkidney
HM06466PIGNtracheaMESH:D005355Fibrosis
HM06466PIGNtracheaMESH:D005885Gingival Hyperplasia
HM06466PIGNtracheaMESH:D007638Keratoconjunctivitis Siccaeye