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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM02973GNStracheaMESH:D005885Gingival Hyperplasia
HM02973GNStracheaMESH:D005355Fibrosis
HM02973GNStracheaMESH:D014820Vitiligobone marrow
HM02973GNStracheaMESH:D009396Wilms Tumorkidney
HM02973GNStracheaMESH:D009396Wilms Tumorcervix
HM02973GNStracheaMESH:D007251Influenza, Human
HM02973GNStracheaMESH:D006258Head and Neck Neoplasmsthyroid
HM02973GNStracheaMESH:D006258Head and Neck Neoplasmsskin
HM02973GNStracheaMESH:D006258Head and Neck Neoplasmsparathyroid gland
HM02973GNStracheaMESH:D006258Head and Neck Neoplasmslarynx
HM02973GNStracheaMESH:D006258Head and Neck Neoplasmsear
HM02973GNStracheaMESH:D006258Head and Neck Neoplasmsbrain
HM02973GNStracheaMESH:D015473Leukemia, Promyelocytic, Acute
HM02973GNStracheaMESH:D007676Kidney Failure, Chronickidney
HM02973GNStracheaMESH:D018236Carcinoma, Embryonal
HM02973GNStracheaMESH:D002294Carcinoma, Squamous Celllung
HM02973GNStracheaMESH:D002294Carcinoma, Squamous Cellliver
HM02973GNStracheaMESH:D002294Carcinoma, Squamous Celllarynx
HM02973GNStracheaMESH:D002294Carcinoma, Squamous Cellkidney
HM02973GNStracheaMESH:D002294Carcinoma, Squamous Celleye
HM02973GNStracheaMESH:D008654Mesotheliomabone
HM02973GNStracheaMESH:D006330Heart Defects, Congenital
HM02973GNStracheaMESH:D005909Glioblastomabone
HM02973GNStracheaMESH:D005909Glioblastomabrain
HM02973GNStracheaMESH:D005909Glioblastomabone
HM02973GNStracheaMESH:D010146Pain
HM02973GNStracheaMESH:D007410Intestinal Diseasessmall intestine
HM02973GNStracheaMESH:D007410Intestinal Diseasesrectum
HM02973GNStracheaMESH:D007410Intestinal Diseasescolon
HM02973GNStracheaMESH:D007410Intestinal Diseasesblood vessel
HM02973GNStracheaMESH:D002583Uterine Cervical Neoplasmscervix
HM02973GNStracheaMESH:D005124Eye Abnormalities
HM02973GNStracheaMESH:D010190Pancreatic Neoplasmspancreas
HM02973GNStracheaMESH:D006317Hearing Loss, Noise-Induced
HM02973GNStracheaMESH:D010051Ovarian Neoplasmsuterus
HM02973GNStracheaMESH:D010051Ovarian Neoplasms
HM02973GNStracheaMESH:D014985Xerophthalmiaeye
HM02973GNStracheaMESH:D017880Limb Deformities, Congenital
HM02973GNStracheaMESH:D009190Myelodysplastic Syndromes
HM02973GNStracheaMESH:D013964Thyroid Neoplasmsthyroid
HM02973GNStracheaMESH:D006457Hemoglobinuria, Paroxysmal
HM02973GNStracheaMESH:D009421Nervous System Malformations
HM02973GNStracheaMESH:D007938Leukemiaspleen
HM02973GNStracheaMESH:D007938Leukemiabone marrow
HM02973GNStracheaMESH:D007638Keratoconjunctivitis Siccaeye
HM02973GNStracheaMESH:D002972Cleft Palate
HM02973GNStracheaMESH:D008527Medulloblastomaembryo
HM02973GNStracheaMESH:D001249Asthmalung
HM02973GNStracheaMESH:D002822Choriocarcinomabrain
HM02973GNStracheaMESH:D014062Tongue Neoplasms
HM02973GNStracheaMESH:D009436Neural Tube Defects
HM02973GNStracheaMESH:D009402Nephrosis, Lipoidkidney
HM02973GNStracheaMESH:D006333Heart Failureheart
HM02973GNStracheaMESH:D010954Plasmacytoma
HM02973GNStracheaMESH:D006973Hypertensionlung
HM02973GNStracheaMESH:D006973Hypertensionheart
HM02973GNStracheaMESH:D006973Hypertensionblood vessel
HM02973GNStracheaMESH:D007951Leukemia, Myeloidbone marrow
HM02973GNStracheaMESH:D014376Tuberculosis
HM02973GNStracheaMESH:D008545Melanomaeye
HM02973GNStracheaMESH:D008545Melanomacervix
HM02973GNStracheaMESH:D008545Melanomabone
HM02973GNStracheaMESH:D056486Drug-Induced Liver Injury
HM02973GNStracheaMESH:D011625Pterygiumeye
HM02973GNStracheaMESH:D014605Uveitiseye
HM02973GNStracheaMESH:D011507Proteinuriakidney
HM02973GNStracheaMESH:D014604Uveal Neoplasmseye
HM02973GNStracheaMESH:D001943Breast Neoplasmsbreast
HM02973GNStracheaMESH:D001778Blood Coagulation Disordersbone marrow
HM02973GNStracheaMESH:D008591Meningomyelocele
HM02973GNStracheaMESH:D011565Psoriasisskin
HM02973GNStracheaMESH:D006930Hyperalgesia
HM02973GNStracheaMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM02973GNStracheaMESH:D017681Hypereosinophilic Syndrome
HM02973GNStracheaMESH:D012208Rhabdomyosarcomarectum
HM02973GNStracheaMESH:D012208Rhabdomyosarcomaprostate
HM02973GNStracheaMESH:D012208Rhabdomyosarcomamuscle
HM02973GNStracheaMESH:D008664Metal Metabolism, Inborn Errorsskin
HM02973GNStracheaMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM02973GNStracheaMESH:D008664Metal Metabolism, Inborn Errorsliver
HM02973GNStracheaMESH:D008664Metal Metabolism, Inborn Errorskidney
HM02973GNStracheaMESH:D003092Colitis
HM02973GNStracheaMESH:D000505Alopeciaskin
HM02973GNStracheaMESH:D007674Kidney Diseasesureter
HM02973GNStracheaMESH:D007674Kidney Diseasespituitary
HM02973GNStracheaMESH:D007674Kidney Diseaseskidney
HM02973GNStracheaMESH:D002386Cataractpancreas
HM02973GNStracheaMESH:D002386Cataracteye
HM02973GNStracheaMESH:D016889Endometrial Neoplasmsuterus
HM02973GNStracheaMESH:D018290Cervical Intraepithelial Neoplasia
HM02973GNStracheaMESH:D012878Skin Neoplasms
HM02973GNStracheaMESH:D019465Craniofacial Abnormalities
HM02973GNStracheaMESH:D008106Liver Cirrhosis, Experimental
HM02973GNStracheaMESH:D009084Mucopolysaccharidosis IIIbone
HM02973GNStracheaMESH:D013274Stomach Neoplasms
HM02973GNStracheaMESH:D006528Carcinoma, Hepatocellularliver
HM02973GNStracheaMESH:D009369Neoplasmsspleen
HM02973GNStracheaMESH:D009369Neoplasmsbone marrow
HM02973GNStracheaMESH:D001169Arthritis, Experimental
HM02973GNStracheaMESH:D001997Bronchopulmonary Dysplasialung
HM02973GNStracheaMESH:D008325Mammary Neoplasms, Experimental
HM02973GNStracheaMESH:D009404Nephrotic Syndromekidney
HM02973GNStracheaMESH:D001172Arthritis, Rheumatoidbone
HM02973GNStracheaMESH:D007569Jaw Abnormalities
HM02973GNStracheaMESH:D001471Barrett Esophagusesophagus