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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06762FGF3colonMESH:D015473Leukemia, Promyelocytic, Acute
HM06762FGF3colonMESH:D001172Arthritis, Rheumatoidbone
HM06762FGF3colonMESH:D001778Blood Coagulation Disordersbone marrow
HM06762FGF3colonMESH:D016889Endometrial Neoplasmsuterus
HM06762FGF3colonMESH:D005355Fibrosis
HM06762FGF3colonMESH:D008545Melanomaeye
HM06762FGF3colonMESH:D008545Melanomacervix
HM06762FGF3colonMESH:D008545Melanomabone
HM06762FGF3colonMESH:D014604Uveal Neoplasmseye
HM06762FGF3colonMESH:D002822Choriocarcinomabrain
HM06762FGF3colonMESH:D001997Bronchopulmonary Dysplasialung
HM06762FGF3colonMESH:D010051Ovarian Neoplasmsuterus
HM06762FGF3colonMESH:D010051Ovarian Neoplasms
HM06762FGF3colonMESH:D008106Liver Cirrhosis, Experimental
HM06762FGF3colonMESH:D002583Uterine Cervical Neoplasmscervix
HM06762FGF3colonMESH:D009369Neoplasmsspleen
HM06762FGF3colonMESH:D009369Neoplasmsbone marrow
HM06762FGF3colonMESH:D006319Hearing Loss, Sensorineural
HM06762FGF3colonMESH:D014062Tongue Neoplasms
HM06762FGF3colonMESH:D009190Myelodysplastic Syndromes
HM06762FGF3colonMESH:D011625Pterygiumeye
HM06762FGF3colonMESH:D012878Skin Neoplasms
HM06762FGF3colonMESH:D018290Cervical Intraepithelial Neoplasia
HM06762FGF3colonMESH:D013964Thyroid Neoplasmsthyroid
HM06762FGF3colonMESH:D000505Alopeciaskin
HM06762FGF3colonMESH:D006528Carcinoma, Hepatocellularliver
HM06762FGF3colonMESH:D001471Barrett Esophagusesophagus
HM06762FGF3colonOMIM:610706DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA
HM06762FGF3colonMESH:D006258Head and Neck Neoplasmsthyroid
HM06762FGF3colonMESH:D006258Head and Neck Neoplasmsskin
HM06762FGF3colonMESH:D006258Head and Neck Neoplasmsparathyroid gland
HM06762FGF3colonMESH:D006258Head and Neck Neoplasmslarynx
HM06762FGF3colonMESH:D006258Head and Neck Neoplasmsear
HM06762FGF3colonMESH:D006258Head and Neck Neoplasmsbrain
HM06762FGF3colonMESH:D012851Sinus Thrombosis, Intracranialblood vessel
HM06762FGF3colonMESH:D007569Jaw Abnormalities
HM06762FGF3colonMESH:D001943Breast Neoplasmsbreast
HM06762FGF3colonMESH:D005909Glioblastomabone
HM06762FGF3colonMESH:D005909Glioblastomabrain
HM06762FGF3colonMESH:D005909Glioblastomabone
HM06762FGF3colonMESH:D009436Neural Tube Defects
HM06762FGF3colonMESH:D014657Vasculitiseye
HM06762FGF3colonMESH:D014657Vasculitisbone marrow
HM06762FGF3colonMESH:D014657Vasculitisblood vessel
HM06762FGF3colonMESH:D002972Cleft Palate
HM06762FGF3colonMESH:D008591Meningomyelocele
HM06762FGF3colonMESH:D014820Vitiligobone marrow
HM06762FGF3colonMESH:D018236Carcinoma, Embryonal
HM06762FGF3colonMESH:D003092Colitis
HM06762FGF3colonMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM06762FGF3colonMESH:D012208Rhabdomyosarcomarectum
HM06762FGF3colonMESH:D012208Rhabdomyosarcomaprostate
HM06762FGF3colonMESH:D012208Rhabdomyosarcomamuscle
HM06762FGF3colonMESH:D009396Wilms Tumorkidney
HM06762FGF3colonMESH:D009396Wilms Tumorcervix
HM06762FGF3colonMESH:D010146Pain
HM06762FGF3colonMESH:D009421Nervous System Malformations
HM06762FGF3colonMESH:D002971Cleft Lip
HM06762FGF3colonMESH:D001249Asthmalung
HM06762FGF3colonMESH:D013921Thrombocytopeniakidney
HM06762FGF3colonMESH:D013921Thrombocytopeniabone marrow
HM06762FGF3colonMESH:D009057Stomatognathic Diseases
HM06762FGF3colonMESH:D014376Tuberculosis
HM06762FGF3colonMESH:D017681Hypereosinophilic Syndrome
HM06762FGF3colonMESH:D001169Arthritis, Experimental
HM06762FGF3colonMESH:D007951Leukemia, Myeloidbone marrow
HM06762FGF3colonMESH:D006930Hyperalgesia
HM06762FGF3colonMESH:D011507Proteinuriakidney
HM06762FGF3colonMESH:D019465Craniofacial Abnormalities
HM06762FGF3colonMESH:D002294Carcinoma, Squamous Celllung
HM06762FGF3colonMESH:D002294Carcinoma, Squamous Cellliver
HM06762FGF3colonMESH:D002294Carcinoma, Squamous Celllarynx
HM06762FGF3colonMESH:D002294Carcinoma, Squamous Cellkidney
HM06762FGF3colonMESH:D002294Carcinoma, Squamous Celleye
HM06762FGF3colonMESH:D007938Leukemiaspleen
HM06762FGF3colonMESH:D007938Leukemiabone marrow
HM06762FGF3colonMESH:D013927Thrombosis
HM06762FGF3colonMESH:D010190Pancreatic Neoplasmspancreas
HM06762FGF3colonMESH:D013274Stomach Neoplasms
HM06762FGF3colonMESH:D002386Cataractpancreas
HM06762FGF3colonMESH:D002386Cataracteye
HM06762FGF3colonMESH:D008527Medulloblastomaembryo
HM06762FGF3colonMESH:D005124Eye Abnormalities
HM06762FGF3colonMESH:D006317Hearing Loss, Noise-Induced
HM06762FGF3colonMESH:D006330Heart Defects, Congenital
HM06762FGF3colonMESH:D007410Intestinal Diseasessmall intestine
HM06762FGF3colonMESH:D007410Intestinal Diseasesrectum
HM06762FGF3colonMESH:D007410Intestinal Diseasescolon
HM06762FGF3colonMESH:D007410Intestinal Diseasesblood vessel
HM06762FGF3colonMESH:D017880Limb Deformities, Congenital