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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01326TP53I13stomachMESH:D010146Pain
HM01326TP53I13stomachMESH:D018248Adenoma, Liver Cell
HM01326TP53I13stomachMESH:D006943Hyperglycemia
HM01326TP53I13stomachMESH:D009325Nausea
HM01326TP53I13stomachMESH:D019310Pseudolymphoma
HM01326TP53I13stomachMESH:D008113Liver Neoplasms
HM01326TP53I13stomachMESH:D008113Liver Neoplasms
HM01326TP53I13stomachMESH:D000015Abnormalities, Multiple
HM01326TP53I13stomachMESH:D007674Kidney Diseasesureter
HM01326TP53I13stomachMESH:D007674Kidney Diseasespituitary
HM01326TP53I13stomachMESH:D007674Kidney Diseaseskidney
HM01326TP53I13stomachMESH:D009436Neural Tube Defects
HM01326TP53I13stomachMESH:D001778Blood Coagulation Disordersbone marrow
HM01326TP53I13stomachMESH:D003876Dermatitis, Atopicskin
HM01326TP53I13stomachMESH:D005317Fetal Growth Retardation
HM01326TP53I13stomachMESH:D001008Anxiety Disorders
HM01326TP53I13stomachMESH:D009765Obesity
HM01326TP53I13stomachMESH:D008881Migraine Disordersbrain
HM01326TP53I13stomachMESH:D001848Bone Diseases, Developmental
HM01326TP53I13stomachMESH:D005234Fatty Liver
HM01326TP53I13stomachMESH:D013226Status Epilepticusmuscle
HM01326TP53I13stomachMESH:D013226Status Epilepticusmuscle
HM01326TP53I13stomachMESH:D013226Status Epilepticusmuscle
HM01326TP53I13stomachMESH:D020521Strokeblood vessel
HM01326TP53I13stomachMESH:D006849Hydrocephalusbrain
HM01326TP53I13stomachMESH:D002779Cholestasisliver
HM01326TP53I13stomachMESH:D005909Glioblastomabone
HM01326TP53I13stomachMESH:D005909Glioblastomabrain
HM01326TP53I13stomachMESH:D005909Glioblastomabone
HM01326TP53I13stomachMESH:D003110Colonic Neoplasmscolon
HM01326TP53I13stomachMESH:D007333Insulin Resistance
HM01326TP53I13stomachMESH:D015179Colorectal Neoplasms
HM01326TP53I13stomachMESH:D006261Headache
HM01326TP53I13stomachMESH:D055963Asthma, Aspirin-Induced
HM01326TP53I13stomachMESH:D001932Brain Neoplasmsbrain
HM01326TP53I13stomachMESH:D056486Drug-Induced Liver Injury
HM01326TP53I13stomachMESH:D006973Hypertensionlung
HM01326TP53I13stomachMESH:D006973Hypertensionheart
HM01326TP53I13stomachMESH:D006973Hypertensionblood vessel
HM01326TP53I13stomachMESH:D014178Translocation, Genetic
HM01326TP53I13stomachMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM01326TP53I13stomachMESH:D004828Epilepsies, Partialmuscle
HM01326TP53I13stomachMESH:D009135Muscular Diseasesmuscle
HM01326TP53I13stomachMESH:D009190Myelodysplastic Syndromes
HM01326TP53I13stomachMESH:D009369Neoplasmsspleen
HM01326TP53I13stomachMESH:D009369Neoplasmsbone marrow
HM01326TP53I13stomachMESH:D004421Dystonia
HM01326TP53I13stomachMESH:D014581Urticariaskin
HM01326TP53I13stomachMESH:D000550Amblyopiabrain
HM01326TP53I13stomachMESH:D000550Amblyopiabrain
HM01326TP53I13stomachMESH:D005885Gingival Hyperplasia
HM01326TP53I13stomachMESH:D008664Metal Metabolism, Inborn Errorsskin
HM01326TP53I13stomachMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM01326TP53I13stomachMESH:D008664Metal Metabolism, Inborn Errorsliver
HM01326TP53I13stomachMESH:D008664Metal Metabolism, Inborn Errorskidney
HM01326TP53I13stomachMESH:D020795Photophobia
HM01326TP53I13stomachMESH:D012001Hyperacusis
HM01326TP53I13stomachMESH:D012851Sinus Thrombosis, Intracranialblood vessel
HM01326TP53I13stomachMESH:D020194Unverricht-Lundborg Syndromemuscle
HM01326TP53I13stomachMESH:D004827Epilepsymuscle
HM01326TP53I13stomachMESH:D006529Hepatomegaly
HM01326TP53I13stomachMESH:D017563Lung Diseases, Interstitiallung
HM01326TP53I13stomachMESH:D015428Myocardial Reperfusion Injury
HM01326TP53I13stomachMESH:D010003Osteoarthritisbone
HM01326TP53I13stomachMESH:D015427Reperfusion Injury
HM01326TP53I13stomachMESH:D013927Thrombosis
HM01326TP53I13stomachMESH:D006457Hemoglobinuria, Paroxysmal
HM01326TP53I13stomachMESH:D012220Rhinitis
HM01326TP53I13stomachMESH:D055371Acute Lung Injury
HM01326TP53I13stomachMESH:D007638Keratoconjunctivitis Siccaeye
HM01326TP53I13stomachMESH:D016135Spinal Dysraphismspinal cord
HM01326TP53I13stomachMESH:D000014Abnormalities, Drug-Induced
HM01326TP53I13stomachMESH:D005315Fetal Diseases
HM01326TP53I13stomachMESH:D012208Rhabdomyosarcomarectum
HM01326TP53I13stomachMESH:D012208Rhabdomyosarcomaprostate
HM01326TP53I13stomachMESH:D012208Rhabdomyosarcomamuscle
HM01326TP53I13stomachMESH:D019465Craniofacial Abnormalities
HM01326TP53I13stomachMESH:D017029Epilepsy, Complex Partialmuscle
HM01326TP53I13stomachMESH:D008106Liver Cirrhosis, Experimental
HM01326TP53I13stomachMESH:D001321Autistic Disorder
HM01326TP53I13stomachMESH:D004832Epilepsy, Absencemuscle
HM01326TP53I13stomachMESH:D014605Uveitiseye
HM01326TP53I13stomachMESH:D009402Nephrosis, Lipoidkidney
HM01326TP53I13stomachMESH:D011565Psoriasisskin
HM01326TP53I13stomachMESH:D012559Schizophrenia
HM01326TP53I13stomachMESH:D001943Breast Neoplasmsbreast
HM01326TP53I13stomachMESH:D014985Xerophthalmiaeye
HM01326TP53I13stomachMESH:D004487Edema
HM01326TP53I13stomachMESH:D006333Heart Failureheart
HM01326TP53I13stomachMESH:D001714Bipolar Disorder
HM01326TP53I13stomachMESH:D009404Nephrotic Syndromekidney
HM01326TP53I13stomachMESH:D012640Seizuresmuscle
HM01326TP53I13stomachMESH:D005355Fibrosis
HM01326TP53I13stomachMESH:D009139Musculoskeletal Abnormalities
HM01326TP53I13stomachMESH:D009203Myocardial Infarctionheart
HM01326TP53I13stomachMESH:D010438Peptic Ulcer Hemorrhage
HM01326TP53I13stomachMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM01326TP53I13stomachMESH:D004831Epilepsies, Myoclonicmuscle
HM01326TP53I13stomachMESH:D014564Urogenital Abnormalities