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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM02411FGF17embryoMESH:D013274Stomach Neoplasms
HM02411FGF17embryoMESH:D017449Dermatitis, Allergic Contactskin
HM02411FGF17embryoMESH:D007248Infertility, Male
HM02411FGF17embryoMESH:D001778Blood Coagulation Disordersbone marrow
HM02411FGF17embryoMESH:D019465Craniofacial Abnormalities
HM02411FGF17embryoMESH:D007569Jaw Abnormalities
HM02411FGF17embryoMESH:D017880Limb Deformities, Congenital
HM02411FGF17embryoMESH:D006930Hyperalgesia
HM02411FGF17embryoMESH:D002972Cleft Palate
HM02411FGF17embryoMESH:D009369Neoplasmsspleen
HM02411FGF17embryoMESH:D009369Neoplasmsbone marrow
HM02411FGF17embryoMESH:D012140Respiratory Tract Diseases
HM02411FGF17embryoMESH:D009436Neural Tube Defects
HM02411FGF17embryoMESH:D007951Leukemia, Myeloidbone marrow
HM02411FGF17embryoMESH:D009396Wilms Tumorkidney
HM02411FGF17embryoMESH:D009396Wilms Tumorcervix
HM02411FGF17embryoMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM02411FGF17embryoMESH:D002294Carcinoma, Squamous Celllung
HM02411FGF17embryoMESH:D002294Carcinoma, Squamous Cellliver
HM02411FGF17embryoMESH:D002294Carcinoma, Squamous Celllarynx
HM02411FGF17embryoMESH:D002294Carcinoma, Squamous Cellkidney
HM02411FGF17embryoMESH:D002294Carcinoma, Squamous Celleye
HM02411FGF17embryoMESH:D011041Poisoning
HM02411FGF17embryoMESH:D016889Endometrial Neoplasmsuterus
HM02411FGF17embryoMESH:D010146Pain
HM02411FGF17embryoMESH:D003092Colitis
HM02411FGF17embryoMESH:D005909Glioblastomabone
HM02411FGF17embryoMESH:D005909Glioblastomabrain
HM02411FGF17embryoMESH:D005909Glioblastomabone
HM02411FGF17embryoMESH:D008545Melanomaeye
HM02411FGF17embryoMESH:D008545Melanomacervix
HM02411FGF17embryoMESH:D008545Melanomabone
HM02411FGF17embryoMESH:D009421Nervous System Malformations
HM02411FGF17embryoMESH:D002583Uterine Cervical Neoplasmscervix
HM02411FGF17embryoMESH:D007247Infertility, Female
HM02411FGF17embryoMESH:D007938Leukemiaspleen
HM02411FGF17embryoMESH:D007938Leukemiabone marrow
HM02411FGF17embryoMESH:D010051Ovarian Neoplasmsuterus
HM02411FGF17embryoMESH:D010051Ovarian Neoplasms
HM02411FGF17embryoMESH:D001471Barrett Esophagusesophagus
HM02411FGF17embryoMESH:D008527Medulloblastomaembryo
HM02411FGF17embryoMESH:D014604Uveal Neoplasmseye
HM02411FGF17embryoMESH:D012729Sex Chromosome Aberrations
HM02411FGF17embryoMESH:D002386Cataractpancreas
HM02411FGF17embryoMESH:D002386Cataracteye
HM02411FGF17embryoMESH:D006258Head and Neck Neoplasmsthyroid
HM02411FGF17embryoMESH:D006258Head and Neck Neoplasmsskin
HM02411FGF17embryoMESH:D006258Head and Neck Neoplasmsparathyroid gland
HM02411FGF17embryoMESH:D006258Head and Neck Neoplasmslarynx
HM02411FGF17embryoMESH:D006258Head and Neck Neoplasmsear
HM02411FGF17embryoMESH:D006258Head and Neck Neoplasmsbrain
HM02411FGF17embryoMESH:D000382Agricultural Workers' Diseases
HM02411FGF17embryoMESH:D002822Choriocarcinomabrain
HM02411FGF17embryoMESH:D015658HIV Infections
HM02411FGF17embryoMESH:D008113Liver Neoplasms
HM02411FGF17embryoMESH:D008113Liver Neoplasms
HM02411FGF17embryoMESH:D008591Meningomyelocele
HM02411FGF17embryoMESH:D014062Tongue Neoplasms
HM02411FGF17embryoMESH:D000505Alopeciaskin
HM02411FGF17embryoMESH:D004417Dyspnea
HM02411FGF17embryoMESH:D007410Intestinal Diseasessmall intestine
HM02411FGF17embryoMESH:D007410Intestinal Diseasesrectum
HM02411FGF17embryoMESH:D007410Intestinal Diseasescolon
HM02411FGF17embryoMESH:D007410Intestinal Diseasesblood vessel
HM02411FGF17embryoMESH:D018290Cervical Intraepithelial Neoplasia
HM02411FGF17embryoMESH:D017681Hypereosinophilic Syndrome
HM02411FGF17embryoMESH:D006505Hepatitis
HM02411FGF17embryoMESH:D012878Skin Neoplasms
HM02411FGF17embryoMESH:D006330Heart Defects, Congenital
HM02411FGF17embryoMESH:D001249Asthmalung
HM02411FGF17embryoMESH:D008107Liver Diseasesskin
HM02411FGF17embryoMESH:D008107Liver Diseasesmuscle
HM02411FGF17embryoMESH:D008107Liver Diseaseslung
HM02411FGF17embryoMESH:D008107Liver Diseasesliver
HM02411FGF17embryoMESH:D010190Pancreatic Neoplasmspancreas
HM02411FGF17embryoMESH:D009190Myelodysplastic Syndromes
HM02411FGF17embryoMESH:D001169Arthritis, Experimental
HM02411FGF17embryoMESH:D010300Parkinson Diseasenerve
HM02411FGF17embryoMESH:D011507Proteinuriakidney
HM02411FGF17embryoMESH:D012208Rhabdomyosarcomarectum
HM02411FGF17embryoMESH:D012208Rhabdomyosarcomaprostate
HM02411FGF17embryoMESH:D012208Rhabdomyosarcomamuscle
HM02411FGF17embryoMESH:D013964Thyroid Neoplasmsthyroid
HM02411FGF17embryoMESH:D006528Carcinoma, Hepatocellularliver
HM02411FGF17embryoMESH:D014820Vitiligobone marrow
HM02411FGF17embryoMESH:D015473Leukemia, Promyelocytic, Acute
HM02411FGF17embryoMESH:D005124Eye Abnormalities
HM02411FGF17embryoMESH:D001997Bronchopulmonary Dysplasialung
HM02411FGF17embryoMESH:D011625Pterygiumeye
HM02411FGF17embryoMESH:D014570Urologic Diseases
HM02411FGF17embryoMESH:D001172Arthritis, Rheumatoidbone
HM02411FGF17embryoMESH:D001943Breast Neoplasmsbreast
HM02411FGF17embryoMESH:D014376Tuberculosis
HM02411FGF17embryoMESH:D006317Hearing Loss, Noise-Induced
HM02411FGF17embryoMESH:D012135Respiratory Sounds
HM02411FGF17embryoMESH:D008106Liver Cirrhosis, Experimental
HM02411FGF17embryoMESH:D005355Fibrosis
HM02411FGF17embryoMESH:D020258Neurotoxicity Syndromes
HM02411FGF17embryoMESH:D018236Carcinoma, Embryonal