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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00221FCGR3BbloodMESH:D006505Hepatitis
HM00221FCGR3BbloodMESH:D014605Uveitiseye
HM00221FCGR3BbloodMESH:D000740Anemiabone marrow
HM00221FCGR3BbloodMESH:D009765Obesity
HM00221FCGR3BbloodMESH:D024821Metabolic Syndrome X
HM00221FCGR3BbloodMESH:D015431Weight Loss
HM00221FCGR3BbloodMESH:D006948Hyperkinesis
HM00221FCGR3BbloodMESH:D014890Wegener Granulomatosisbone marrow
HM00221FCGR3BbloodMESH:D001523Mental Disorders
HM00221FCGR3BbloodMESH:D007249Inflammation
HM00221FCGR3BbloodMESH:D000380Agranulocytosisbone marrow
HM00221FCGR3BbloodMESH:D008064Lipidoses
HM00221FCGR3BbloodMESH:D009102Multiple Organ Failure
HM00221FCGR3BbloodMESH:D012559Schizophrenia
HM00221FCGR3BbloodMESH:D003924Diabetes Mellitus, Type 2pancreas
HM00221FCGR3BbloodMESH:D010212Papillomabrain
HM00221FCGR3BbloodMESH:D010212Papillomaliver
HM00221FCGR3BbloodMESH:D010212Papilloma
HM00221FCGR3BbloodMESH:D006970Disorders of Excessive Somnolence
HM00221FCGR3BbloodMESH:D008181Lupus Nephritis
HM00221FCGR3BbloodMESH:D002318Cardiovascular Diseasesheart
HM00221FCGR3BbloodMESH:D002318Cardiovascular Diseasesbone marrow
HM00221FCGR3BbloodMESH:D002318Cardiovascular Diseasesblood vessel
HM00221FCGR3BbloodMESH:D007676Kidney Failure, Chronickidney
HM00221FCGR3BbloodMESH:D050171Dyslipidemias
HM00221FCGR3BbloodMESH:D011618Psychotic Disorders
HM00221FCGR3BbloodMESH:D012878Skin Neoplasms
HM00221FCGR3BbloodMESH:D003072Cognition Disorders
HM00221FCGR3BbloodMESH:D043183Irritable Bowel Syndrome
HM00221FCGR3BbloodMESH:D015430Weight Gain
HM00221FCGR3BbloodMESH:D001169Arthritis, Experimental
HM00221FCGR3BbloodMESH:D004487Edema
HM00221FCGR3BbloodMESH:D010538Peritonitis
HM00221FCGR3BbloodMESH:D018805Sepsis