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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01079CHI3L2boneMESH:D014985Xerophthalmiaeye
HM01079CHI3L2boneMESH:D014605Uveitiseye
HM01079CHI3L2boneMESH:D005355Fibrosis
HM01079CHI3L2boneMESH:D007638Keratoconjunctivitis Siccaeye
HM01079CHI3L2boneMESH:D008664Metal Metabolism, Inborn Errorsskin
HM01079CHI3L2boneMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM01079CHI3L2boneMESH:D008664Metal Metabolism, Inborn Errorsliver
HM01079CHI3L2boneMESH:D008664Metal Metabolism, Inborn Errorskidney
HM01079CHI3L2boneMESH:D011565Psoriasisskin
HM01079CHI3L2boneMESH:D005885Gingival Hyperplasia
HM01079CHI3L2boneMESH:D006973Hypertensionlung
HM01079CHI3L2boneMESH:D006973Hypertensionheart
HM01079CHI3L2boneMESH:D006973Hypertensionblood vessel
HM01079CHI3L2boneMESH:D007674Kidney Diseasesureter
HM01079CHI3L2boneMESH:D007674Kidney Diseasespituitary
HM01079CHI3L2boneMESH:D007674Kidney Diseaseskidney
HM01079CHI3L2boneMESH:D006457Hemoglobinuria, Paroxysmal
HM01079CHI3L2boneMESH:D009404Nephrotic Syndromekidney
HM01079CHI3L2boneMESH:D009402Nephrosis, Lipoidkidney