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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05003GIMAP5pharynxMESH:D020521Strokeblood vessel
HM05003GIMAP5pharynxMESH:D019584Hot Flashes
HM05003GIMAP5pharynxMESH:D012559Schizophrenia
HM05003GIMAP5pharynxMESH:D001943Breast Neoplasmsbreast
HM05003GIMAP5pharynxMESH:D006330Heart Defects, Congenital
HM05003GIMAP5pharynxMESH:D001862Bone Resorption
HM05003GIMAP5pharynxMESH:D007674Kidney Diseasesureter
HM05003GIMAP5pharynxMESH:D007674Kidney Diseasespituitary
HM05003GIMAP5pharynxMESH:D007674Kidney Diseaseskidney
HM05003GIMAP5pharynxMESH:D008546Melanoma, Experimental
HM05003GIMAP5pharynxMESH:D016757Death, Sudden, Cardiac
HM05003GIMAP5pharynxMESH:D006948Hyperkinesis
HM05003GIMAP5pharynxMESH:D000799Angioedemaskin
HM05003GIMAP5pharynxMESH:D005832Genital Diseases, Maletestis
HM05003GIMAP5pharynxMESH:D005832Genital Diseases, Maleprostate
HM05003GIMAP5pharynxMESH:D005832Genital Diseases, Maleblood vessel
HM05003GIMAP5pharynxMESH:D015431Weight Loss
HM05003GIMAP5pharynxMESH:D010049Ovarian Diseasesovary
HM05003GIMAP5pharynxMESH:D014581Urticariaskin
HM05003GIMAP5pharynxMESH:D001321Autistic Disorder
HM05003GIMAP5pharynxMESH:D006548Hernia, Diaphragmatic
HM05003GIMAP5pharynxMESH:D011618Psychotic Disorders
HM05003GIMAP5pharynxMESH:D050171Dyslipidemias
HM05003GIMAP5pharynxMESH:D011629Puberty, Precocious
HM05003GIMAP5pharynxMESH:D017180Tachycardia, Ventricular
HM05003GIMAP5pharynxMESH:D019966Substance-Related Disorders
HM05003GIMAP5pharynxMESH:D019636Neurodegenerative Diseasesnerve
HM05003GIMAP5pharynxMESH:D015430Weight Gain
HM05003GIMAP5pharynxMESH:D008175Lung Neoplasmslung
HM05003GIMAP5pharynxMESH:D010146Pain
HM05003GIMAP5pharynxMESH:D014591Uterine Diseasesuterus
HM05003GIMAP5pharynxMESH:D014591Uterine Diseasesplacenta
HM05003GIMAP5pharynxMESH:D014591Uterine Diseasescervix
HM05003GIMAP5pharynxMESH:D008106Liver Cirrhosis, Experimental
HM05003GIMAP5pharynxMESH:D009421Nervous System Malformations
HM05003GIMAP5pharynxMESH:D011472Prostatitisprostate
HM05003GIMAP5pharynxMESH:D007333Insulin Resistance
HM05003GIMAP5pharynxMESH:D008107Liver Diseasesskin
HM05003GIMAP5pharynxMESH:D008107Liver Diseasesmuscle
HM05003GIMAP5pharynxMESH:D008107Liver Diseaseslung
HM05003GIMAP5pharynxMESH:D008107Liver Diseasesliver
HM05003GIMAP5pharynxMESH:D024821Metabolic Syndrome X
HM05003GIMAP5pharynxMESH:D000380Agranulocytosisbone marrow
HM05003GIMAP5pharynxMESH:D007251Influenza, Human
HM05003GIMAP5pharynxMESH:D001523Mental Disorders
HM05003GIMAP5pharynxMESH:D002252Carbon Tetrachloride Poisoning
HM05003GIMAP5pharynxMESH:D056486Drug-Induced Liver Injury
HM05003GIMAP5pharynxMESH:D002278Carcinoma in Situ
HM05003GIMAP5pharynxMESH:D002278Carcinoma in Situ
HM05003GIMAP5pharynxMESH:D007984Leydig Cell Tumor
HM05003GIMAP5pharynxMESH:D003456Cryptorchidism
HM05003GIMAP5pharynxMESH:D009765Obesity
HM05003GIMAP5pharynxMESH:D001008Anxiety Disorders
HM05003GIMAP5pharynxMESH:D002386Cataractpancreas
HM05003GIMAP5pharynxMESH:D002386Cataracteye
HM05003GIMAP5pharynxMESH:D002375Catalepsy
HM05003GIMAP5pharynxMESH:D030342Genetic Diseases, Inborn
HM05003GIMAP5pharynxMESH:D008171Lung Diseases
HM05003GIMAP5pharynxMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM05003GIMAP5pharynxMESH:D003704Dementianerve
HM05003GIMAP5pharynxMESH:D003704Dementiablood vessel
HM05003GIMAP5pharynxMESH:D017114Liver Failure, Acute
HM05003GIMAP5pharynxMESH:D007248Infertility, Male
HM05003GIMAP5pharynxMESH:D009041Motion Sickness
HM05003GIMAP5pharynxMESH:D011471Prostatic Neoplasmsprostate
HM05003GIMAP5pharynxMESH:D003072Cognition Disorders
HM05003GIMAP5pharynxMESH:D006930Hyperalgesia
HM05003GIMAP5pharynxMESH:D011595Psychomotor Agitation
HM05003GIMAP5pharynxMESH:D008064Lipidoses
HM05003GIMAP5pharynxMESH:D011297Prenatal Exposure Delayed Effects
HM05003GIMAP5pharynxMESH:D003924Diabetes Mellitus, Type 2pancreas
HM05003GIMAP5pharynxMESH:D011469Prostatic Diseasesureter
HM05003GIMAP5pharynxMESH:D011469Prostatic Diseasesprostate
HM05003GIMAP5pharynxMESH:D019465Craniofacial Abnormalities
HM05003GIMAP5pharynxMESH:D006970Disorders of Excessive Somnolence