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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01850MTDHlymph nodeMESH:D007674Kidney Diseasesureter
HM01850MTDHlymph nodeMESH:D007674Kidney Diseasespituitary
HM01850MTDHlymph nodeMESH:D007674Kidney Diseaseskidney
HM01850MTDHlymph nodeMESH:D005355Fibrosis
HM01850MTDHlymph nodeMESH:D004938Esophageal Neoplasms
HM01850MTDHlymph nodeMESH:D002471Cell Transformation, Neoplastic
HM01850MTDHlymph nodeMESH:D009402Nephrosis, Lipoidkidney
HM01850MTDHlymph nodeMESH:D014985Xerophthalmiaeye
HM01850MTDHlymph nodeMESH:D008664Metal Metabolism, Inborn Errorsskin
HM01850MTDHlymph nodeMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM01850MTDHlymph nodeMESH:D008664Metal Metabolism, Inborn Errorsliver
HM01850MTDHlymph nodeMESH:D008664Metal Metabolism, Inborn Errorskidney
HM01850MTDHlymph nodeMESH:D001943Breast Neoplasmsbreast
HM01850MTDHlymph nodeMESH:D014605Uveitiseye
HM01850MTDHlymph nodeMESH:D006973Hypertensionlung
HM01850MTDHlymph nodeMESH:D006973Hypertensionheart
HM01850MTDHlymph nodeMESH:D006973Hypertensionblood vessel
HM01850MTDHlymph nodeMESH:D009362Neoplasm Metastasis
HM01850MTDHlymph nodeMESH:D005885Gingival Hyperplasia
HM01850MTDHlymph nodeMESH:D007638Keratoconjunctivitis Siccaeye
HM01850MTDHlymph nodeMESH:D009404Nephrotic Syndromekidney
HM01850MTDHlymph nodeMESH:D006457Hemoglobinuria, Paroxysmal
HM01850MTDHlymph nodeMESH:D011565Psoriasisskin