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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06443FAT3embryoMESH:D012220Rhinitis
HM06443FAT3embryoMESH:D008881Migraine Disordersbrain
HM06443FAT3embryoMESH:D013927Thrombosis
HM06443FAT3embryoMESH:D020521Strokeblood vessel
HM06443FAT3embryoMESH:D010438Peptic Ulcer Hemorrhage
HM06443FAT3embryoMESH:D001932Brain Neoplasmsbrain
HM06443FAT3embryoMESH:D006261Headache
HM06443FAT3embryoMESH:D015179Colorectal Neoplasms
HM06443FAT3embryoMESH:D014581Urticariaskin
HM06443FAT3embryoMESH:D004487Edema
HM06443FAT3embryoMESH:D009203Myocardial Infarctionheart
HM06443FAT3embryoMESH:D010146Pain
HM06443FAT3embryoMESH:D009325Nausea
HM06443FAT3embryoMESH:D010003Osteoarthritisbone
HM06443FAT3embryoMESH:D012001Hyperacusis
HM06443FAT3embryoMESH:D020795Photophobia
HM06443FAT3embryoMESH:D055963Asthma, Aspirin-Induced
HM06443FAT3embryoMESH:D001943Breast Neoplasmsbreast
HM06443FAT3embryoMESH:D003110Colonic Neoplasmscolon
HM06443FAT3embryoMESH:D005909Glioblastomabone
HM06443FAT3embryoMESH:D005909Glioblastomabrain
HM06443FAT3embryoMESH:D005909Glioblastomabone
HM06443FAT3embryoMESH:D012851Sinus Thrombosis, Intracranialblood vessel