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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM02848SLC33A1tracheaMESH:D005355Fibrosis
HM02848SLC33A1tracheaMESH:D007638Keratoconjunctivitis Siccaeye
HM02848SLC33A1tracheaMESH:D006457Hemoglobinuria, Paroxysmal
HM02848SLC33A1tracheaMESH:D011565Psoriasisskin
HM02848SLC33A1tracheaOMIM:612539SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT
HM02848SLC33A1tracheaMESH:D014605Uveitiseye
HM02848SLC33A1tracheaMESH:D006973Hypertensionlung
HM02848SLC33A1tracheaMESH:D006973Hypertensionheart
HM02848SLC33A1tracheaMESH:D006973Hypertensionblood vessel
HM02848SLC33A1tracheaMESH:D008664Metal Metabolism, Inborn Errorsskin
HM02848SLC33A1tracheaMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM02848SLC33A1tracheaMESH:D008664Metal Metabolism, Inborn Errorsliver
HM02848SLC33A1tracheaMESH:D008664Metal Metabolism, Inborn Errorskidney
HM02848SLC33A1tracheaMESH:D009404Nephrotic Syndromekidney
HM02848SLC33A1tracheaMESH:D005885Gingival Hyperplasia
HM02848SLC33A1tracheaMESH:D009402Nephrosis, Lipoidkidney
HM02848SLC33A1tracheaMESH:D014985Xerophthalmiaeye
HM02848SLC33A1tracheaMESH:D007674Kidney Diseasesureter
HM02848SLC33A1tracheaMESH:D007674Kidney Diseasespituitary
HM02848SLC33A1tracheaMESH:D007674Kidney Diseaseskidney