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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04729B3GNT3colonMESH:D001172Arthritis, Rheumatoidbone
HM04729B3GNT3colonMESH:D008223Lymphoma
HM04729B3GNT3colonMESH:D011565Psoriasisskin
HM04729B3GNT3colonMESH:D001161Arteriosclerosisblood vessel
HM04729B3GNT3colonMESH:D008103Liver Cirrhosisliver
HM04729B3GNT3colonMESH:D001943Breast Neoplasmsbreast
HM04729B3GNT3colonMESH:D003550Cystic Fibrosis
HM04729B3GNT3colonMESH:D019851Thrombophiliabone marrow
HM04729B3GNT3colonMESH:D013088Spermatocele
HM04729B3GNT3colonMESH:D017563Lung Diseases, Interstitiallung
HM04729B3GNT3colonMESH:D000152Acne Vulgaris
HM04729B3GNT3colonMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM04729B3GNT3colonMESH:D011537Pruritus
HM04729B3GNT3colonMESH:D051437Renal Insufficiency
HM04729B3GNT3colonMESH:D020246Venous Thrombosis
HM04729B3GNT3colonMESH:D000230Adenocarcinoma
HM04729B3GNT3colonMESH:D000230Adenocarcinomauterus
HM04729B3GNT3colonMESH:D000230Adenocarcinoma
HM04729B3GNT3colonMESH:D000230Adenocarcinoma
HM04729B3GNT3colonMESH:D000230Adenocarcinomauterus
HM04729B3GNT3colonMESH:D000230Adenocarcinomathyroid
HM04729B3GNT3colonMESH:D000230Adenocarcinomaskin
HM04729B3GNT3colonMESH:D000230Adenocarcinomaparathyroid gland
HM04729B3GNT3colonMESH:D000230Adenocarcinomaliver
HM04729B3GNT3colonMESH:D000230Adenocarcinomakidney
HM04729B3GNT3colonMESH:D000230Adenocarcinomaeye
HM04729B3GNT3colonMESH:D000230Adenocarcinomaadrenal gland
HM04729B3GNT3colonMESH:D006086Graft vs Host Disease
HM04729B3GNT3colonMESH:D007248Infertility, Male
HM04729B3GNT3colonMESH:D007021Hypospadias
HM04729B3GNT3colonMESH:D013576Syndactylybone
HM04729B3GNT3colonMESH:D016584Panic Disorder
HM04729B3GNT3colonMESH:D014594Uterine Neoplasmscervix
HM04729B3GNT3colonMESH:D014594Uterine Neoplasms
HM04729B3GNT3colonMESH:D005234Fatty Liver
HM04729B3GNT3colonMESH:D001169Arthritis, Experimental
HM04729B3GNT3colonMESH:D002779Cholestasisliver
HM04729B3GNT3colonMESH:D019465Craniofacial Abnormalities
HM04729B3GNT3colonMESH:D003882Dermatomyositisskin
HM04729B3GNT3colonMESH:D000014Abnormalities, Drug-Induced
HM04729B3GNT3colonMESH:D007805Language Development Disorders
HM04729B3GNT3colonMESH:D007247Infertility, Female
HM04729B3GNT3colonMESH:D052016Mucositis
HM04729B3GNT3colonMESH:D013927Thrombosis