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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06524GNPATtonsilMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM06524GNPATtonsilMESH:D004832Epilepsy, Absencemuscle
HM06524GNPATtonsilMESH:D005756Gastritis
HM06524GNPATtonsilMESH:D006930Hyperalgesia
HM06524GNPATtonsilMESH:D010382Peliosis Hepatisliver
HM06524GNPATtonsilMESH:D003876Dermatitis, Atopicskin
HM06524GNPATtonsilMESH:D056486Drug-Induced Liver Injury
HM06524GNPATtonsilMESH:D006869Hydronephrosiskidney
HM06524GNPATtonsilMESH:D008114Liver Neoplasms, Experimental
HM06524GNPATtonsilMESH:D011297Prenatal Exposure Delayed Effects
HM06524GNPATtonsilMESH:D017119Porphyria Cutanea Tardaskin
HM06524GNPATtonsilMESH:D001943Breast Neoplasmsbreast
HM06524GNPATtonsilMESH:D005313Fetal Death
HM06524GNPATtonsilMESH:D004421Dystonia
HM06524GNPATtonsilMESH:D019310Pseudolymphoma
HM06524GNPATtonsilMESH:D009135Muscular Diseasesmuscle
HM06524GNPATtonsilMESH:D002493Central Nervous System Diseasesspinal cord
HM06524GNPATtonsilMESH:D002493Central Nervous System Diseasesskin
HM06524GNPATtonsilMESH:D002493Central Nervous System Diseasesnerve
HM06524GNPATtonsilMESH:D002493Central Nervous System Diseasesmuscle
HM06524GNPATtonsilMESH:D002493Central Nervous System Diseaseseye
HM06524GNPATtonsilMESH:D002493Central Nervous System Diseasesbrain
HM06524GNPATtonsilMESH:D002971Cleft Lip
HM06524GNPATtonsilMESH:D007333Insulin Resistance
HM06524GNPATtonsilMESH:D019851Thrombophiliabone marrow
HM06524GNPATtonsilMESH:D054079Vascular Malformations
HM06524GNPATtonsilMESH:D000740Anemiabone marrow
HM06524GNPATtonsilMESH:D008104Liver Cirrhosis, Alcoholicliver
HM06524GNPATtonsilMESH:D008113Liver Neoplasms
HM06524GNPATtonsilMESH:D008113Liver Neoplasms
HM06524GNPATtonsilMESH:D017563Lung Diseases, Interstitiallung
HM06524GNPATtonsilMESH:D001321Autistic Disorder
HM06524GNPATtonsilMESH:D006528Carcinoma, Hepatocellularliver
HM06524GNPATtonsilMESH:D015427Reperfusion Injury
HM06524GNPATtonsilMESH:D006470Hemorrhage
HM06524GNPATtonsilMESH:D006943Hyperglycemia
HM06524GNPATtonsilMESH:D000013Congenital Abnormalities
HM06524GNPATtonsilMESH:D003924Diabetes Mellitus, Type 2pancreas
HM06524GNPATtonsilMESH:D000550Amblyopiabrain
HM06524GNPATtonsilMESH:D000550Amblyopiabrain
HM06524GNPATtonsilMESH:D004831Epilepsies, Myoclonicmuscle
HM06524GNPATtonsilMESH:D011537Pruritus
HM06524GNPATtonsilMESH:D004487Edema
HM06524GNPATtonsilMESH:D010190Pancreatic Neoplasmspancreas
HM06524GNPATtonsilMESH:D014594Uterine Neoplasmscervix
HM06524GNPATtonsilMESH:D014594Uterine Neoplasms
HM06524GNPATtonsilMESH:D008103Liver Cirrhosisliver
HM06524GNPATtonsilMESH:D009190Myelodysplastic Syndromes
HM06524GNPATtonsilMESH:D017202Myocardial Ischemiaheart
HM06524GNPATtonsilMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM06524GNPATtonsilMESH:D001778Blood Coagulation Disordersbone marrow
HM06524GNPATtonsilMESH:D009369Neoplasmsspleen
HM06524GNPATtonsilMESH:D009369Neoplasmsbone marrow
HM06524GNPATtonsilMESH:D001848Bone Diseases, Developmental
HM06524GNPATtonsilMESH:D002056Burns
HM06524GNPATtonsilMESH:D008881Migraine Disordersbrain
HM06524GNPATtonsilMESH:D009421Nervous System Malformations
HM06524GNPATtonsilMESH:D000014Abnormalities, Drug-Induced
HM06524GNPATtonsilMESH:D000152Acne Vulgaris
HM06524GNPATtonsilMESH:D001714Bipolar Disorder
HM06524GNPATtonsilMESH:D008107Liver Diseasesskin
HM06524GNPATtonsilMESH:D008107Liver Diseasesmuscle
HM06524GNPATtonsilMESH:D008107Liver Diseaseslung
HM06524GNPATtonsilMESH:D008107Liver Diseasesliver
HM06524GNPATtonsilMESH:D007247Infertility, Female
HM06524GNPATtonsilMESH:D012640Seizuresmuscle
HM06524GNPATtonsilMESH:D000230Adenocarcinoma
HM06524GNPATtonsilMESH:D000230Adenocarcinomauterus
HM06524GNPATtonsilMESH:D000230Adenocarcinoma
HM06524GNPATtonsilMESH:D000230Adenocarcinoma
HM06524GNPATtonsilMESH:D000230Adenocarcinomauterus
HM06524GNPATtonsilMESH:D000230Adenocarcinomathyroid
HM06524GNPATtonsilMESH:D000230Adenocarcinomaskin
HM06524GNPATtonsilMESH:D000230Adenocarcinomaparathyroid gland
HM06524GNPATtonsilMESH:D000230Adenocarcinomaliver
HM06524GNPATtonsilMESH:D000230Adenocarcinomakidney
HM06524GNPATtonsilMESH:D000230Adenocarcinomaeye
HM06524GNPATtonsilMESH:D000230Adenocarcinomaadrenal gland
HM06524GNPATtonsilMESH:D012208Rhabdomyosarcomarectum
HM06524GNPATtonsilMESH:D012208Rhabdomyosarcomaprostate
HM06524GNPATtonsilMESH:D012208Rhabdomyosarcomamuscle
HM06524GNPATtonsilMESH:D001161Arteriosclerosisblood vessel
HM06524GNPATtonsilMESH:D016135Spinal Dysraphismspinal cord
HM06524GNPATtonsilMESH:D006332Cardiomegaly
HM06524GNPATtonsilMESH:D014564Urogenital Abnormalities
HM06524GNPATtonsilMESH:D019465Craniofacial Abnormalities
HM06524GNPATtonsilMESH:D006849Hydrocephalusbrain
HM06524GNPATtonsilMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM06524GNPATtonsilMESH:D004827Epilepsymuscle
HM06524GNPATtonsilMESH:D012878Skin Neoplasms
HM06524GNPATtonsilMESH:D018281Cholangiocarcinomaliver
HM06524GNPATtonsilMESH:D009203Myocardial Infarctionheart
HM06524GNPATtonsilMESH:D005355Fibrosis
HM06524GNPATtonsilMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM06524GNPATtonsilMESH:D001169Arthritis, Experimental
HM06524GNPATtonsilMESH:D020191Myoclonic Epilepsies, Progressivenerve
HM06524GNPATtonsilMESH:D020191Myoclonic Epilepsies, Progressivemuscle
HM06524GNPATtonsilMESH:D013927Thrombosis
HM06524GNPATtonsilMESH:D013959Thyroid Diseasesthyroid
HM06524GNPATtonsilMESH:D002779Cholestasisliver
HM06524GNPATtonsilMESH:D004489Edema, Cardiac
HM06524GNPATtonsilMESH:D007249Inflammation
HM06524GNPATtonsilMESH:D009139Musculoskeletal Abnormalities
HM06524GNPATtonsilMESH:D009436Neural Tube Defects
HM06524GNPATtonsilMESH:D000853Anophthalmos
HM06524GNPATtonsilMESH:D013088Spermatocele
HM06524GNPATtonsilMESH:D020194Unverricht-Lundborg Syndromemuscle
HM06524GNPATtonsilMESH:D019282Wasting Syndrome
HM06524GNPATtonsilMESH:D012559Schizophrenia
HM06524GNPATtonsilMESH:D005235Fatty Liver, Alcoholic
HM06524GNPATtonsilMESH:D009765Obesity
HM06524GNPATtonsilMESH:D015428Myocardial Reperfusion Injury
HM06524GNPATtonsilMESH:D013375Substance Withdrawal Syndrome
HM06524GNPATtonsilMESH:D002972Cleft Palate
HM06524GNPATtonsilMESH:D004938Esophageal Neoplasms
HM06524GNPATtonsilMESH:D005124Eye Abnormalities
HM06524GNPATtonsilMESH:D007021Hypospadias
HM06524GNPATtonsilMESH:D007859Learning Disorders
HM06524GNPATtonsilMESH:D013226Status Epilepticusmuscle
HM06524GNPATtonsilMESH:D013226Status Epilepticusmuscle
HM06524GNPATtonsilMESH:D013226Status Epilepticusmuscle
HM06524GNPATtonsilMESH:D020246Venous Thrombosis
HM06524GNPATtonsilMESH:D001008Anxiety Disorders
HM06524GNPATtonsilMESH:D007248Infertility, Male
HM06524GNPATtonsilMESH:D008569Memory Disorders
HM06524GNPATtonsilMESH:D010018Osteomalaciabone
HM06524GNPATtonsilMESH:D005234Fatty Liver
HM06524GNPATtonsilMESH:D006973Hypertensionlung
HM06524GNPATtonsilMESH:D006973Hypertensionheart
HM06524GNPATtonsilMESH:D006973Hypertensionblood vessel
HM06524GNPATtonsilMESH:D055371Acute Lung Injury
HM06524GNPATtonsilMESH:D008175Lung Neoplasmslung
HM06524GNPATtonsilMESH:D016584Panic Disorder
HM06524GNPATtonsilMESH:D013276Stomach Ulcer
HM06524GNPATtonsilMESH:D000015Abnormalities, Multiple
HM06524GNPATtonsilMESH:D005317Fetal Growth Retardation
HM06524GNPATtonsilMESH:D008108Liver Diseases, Alcoholic
HM06524GNPATtonsilMESH:C537607Rhizomelic chondrodysplasia punctata, type 2
HM06524GNPATtonsilMESH:D004362Drug Toxicity
HM06524GNPATtonsilMESH:D017029Epilepsy, Complex Partialmuscle
HM06524GNPATtonsilMESH:D015619Respiratory System Abnormalities
HM06524GNPATtonsilMESH:D014178Translocation, Genetic
HM06524GNPATtonsilMESH:D004828Epilepsies, Partialmuscle
HM06524GNPATtonsilMESH:D005315Fetal Diseases
HM06524GNPATtonsilMESH:D005310Fetal Alcohol Syndrome
HM06524GNPATtonsilMESH:D007569Jaw Abnormalities
HM06524GNPATtonsilMESH:D001836Body Weight Changes
HM06524GNPATtonsilMESH:D006529Hepatomegaly
HM06524GNPATtonsilMESH:D020268Alcohol-Induced Disorders, Nervous System
HM06524GNPATtonsilMESH:D011230Precancerous Conditions
HM06524GNPATtonsilMESH:D008106Liver Cirrhosis, Experimental
HM06524GNPATtonsilMESH:D003294Seizures, Febrile
HM06524GNPATtonsilMESH:D018248Adenoma, Liver Cell
HM06524GNPATtonsilMESH:D002277Carcinoma
HM06524GNPATtonsilMESH:D006330Heart Defects, Congenital
HM06524GNPATtonsilMESH:D017880Limb Deformities, Congenital
HM06524GNPATtonsilMESH:D006333Heart Failureheart