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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05367F12stomachMESH:D009232Myxoma
HM05367F12stomachMESH:D012559Schizophrenia
HM05367F12stomachMESH:D006086Graft vs Host Disease
HM05367F12stomachMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM05367F12stomachMESH:D008103Liver Cirrhosisliver
HM05367F12stomachMESH:D009190Myelodysplastic Syndromes
HM05367F12stomachMESH:D001778Blood Coagulation Disordersbone marrow
HM05367F12stomachMESH:D009139Musculoskeletal Abnormalities
HM05367F12stomachMESH:D002277Carcinoma
HM05367F12stomachMESH:D004421Dystonia
HM05367F12stomachMESH:D009062Mouth Neoplasms
HM05367F12stomachMESH:D012640Seizuresmuscle
HM05367F12stomachMESH:D017029Epilepsy, Complex Partialmuscle
HM05367F12stomachMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM05367F12stomachMESH:D008223Lymphoma
HM05367F12stomachMESH:D018200Mixed Tumor, Mullerianbone
HM05367F12stomachMESH:D011297Prenatal Exposure Delayed Effects
HM05367F12stomachMESH:D002583Uterine Cervical Neoplasmscervix
HM05367F12stomachMESH:D001848Bone Diseases, Developmental
HM05367F12stomachMESH:D006528Carcinoma, Hepatocellularliver
HM05367F12stomachMESH:D000015Abnormalities, Multiple
HM05367F12stomachMESH:D001172Arthritis, Rheumatoidbone
HM05367F12stomachMESH:D005234Fatty Liver
HM05367F12stomachMESH:D020194Unverricht-Lundborg Syndromemuscle
HM05367F12stomachMESH:D013576Syndactylybone
HM05367F12stomachMESH:D006869Hydronephrosiskidney
HM05367F12stomachMESH:D014178Translocation, Genetic
HM05367F12stomachMESH:D008113Liver Neoplasms
HM05367F12stomachMESH:D008113Liver Neoplasms
HM05367F12stomachMESH:D013226Status Epilepticusmuscle
HM05367F12stomachMESH:D013226Status Epilepticusmuscle
HM05367F12stomachMESH:D013226Status Epilepticusmuscle
HM05367F12stomachMESH:D011565Psoriasisskin
HM05367F12stomachMESH:D051437Renal Insufficiency
HM05367F12stomachMESH:D054556Venous Thromboembolism
HM05367F12stomachMESH:D007680Kidney Neoplasmskidney
HM05367F12stomachMESH:D054079Vascular Malformations
HM05367F12stomachMESH:D056486Drug-Induced Liver Injury
HM05367F12stomachMESH:D009101Multiple Myelomabone marrow
HM05367F12stomachMESH:D020521Strokeblood vessel
HM05367F12stomachMESH:D017563Lung Diseases, Interstitiallung
HM05367F12stomachMESH:D012208Rhabdomyosarcomarectum
HM05367F12stomachMESH:D012208Rhabdomyosarcomaprostate
HM05367F12stomachMESH:D012208Rhabdomyosarcomamuscle
HM05367F12stomachMESH:D000419Albuminuria
HM05367F12stomachMESH:D018281Cholangiocarcinomaliver
HM05367F12stomachMESH:D005175Factor XII Deficiency
HM05367F12stomachMESH:D005317Fetal Growth Retardation
HM05367F12stomachMESH:D005885Gingival Hyperplasia
HM05367F12stomachMESH:D016135Spinal Dysraphismspinal cord
HM05367F12stomachMESH:D009404Nephrotic Syndromekidney
HM05367F12stomachMESH:D001930Brain Injuries
HM05367F12stomachMESH:D002294Carcinoma, Squamous Celllung
HM05367F12stomachMESH:D002294Carcinoma, Squamous Cellliver
HM05367F12stomachMESH:D002294Carcinoma, Squamous Celllarynx
HM05367F12stomachMESH:D002294Carcinoma, Squamous Cellkidney
HM05367F12stomachMESH:D002294Carcinoma, Squamous Celleye
HM05367F12stomachMESH:D000013Congenital Abnormalities
HM05367F12stomachMESH:D004828Epilepsies, Partialmuscle
HM05367F12stomachMESH:D004938Esophageal Neoplasms
HM05367F12stomachMESH:D005315Fetal Diseases
HM05367F12stomachMESH:D007569Jaw Abnormalities
HM05367F12stomachMESH:D009369Neoplasmsspleen
HM05367F12stomachMESH:D009369Neoplasmsbone marrow
HM05367F12stomachMESH:D009402Nephrosis, Lipoidkidney
HM05367F12stomachMESH:D001943Breast Neoplasmsbreast
HM05367F12stomachMESH:D007644Darier Diseaseskin
HM05367F12stomachMESH:D005124Eye Abnormalities
HM05367F12stomachMESH:D008178Lupus Erythematosus, Cutaneous
HM05367F12stomachMESH:D000014Abnormalities, Drug-Induced
HM05367F12stomachMESH:D001321Autistic Disorder
HM05367F12stomachMESH:D004831Epilepsies, Myoclonicmuscle
HM05367F12stomachMESH:D007674Kidney Diseasesureter
HM05367F12stomachMESH:D007674Kidney Diseasespituitary
HM05367F12stomachMESH:D007674Kidney Diseaseskidney
HM05367F12stomachMESH:D014062Tongue Neoplasms
HM05367F12stomachMESH:D000230Adenocarcinoma
HM05367F12stomachMESH:D000230Adenocarcinomauterus
HM05367F12stomachMESH:D000230Adenocarcinoma
HM05367F12stomachMESH:D000230Adenocarcinoma
HM05367F12stomachMESH:D000230Adenocarcinomauterus
HM05367F12stomachMESH:D000230Adenocarcinomathyroid
HM05367F12stomachMESH:D000230Adenocarcinomaskin
HM05367F12stomachMESH:D000230Adenocarcinomaparathyroid gland
HM05367F12stomachMESH:D000230Adenocarcinomaliver
HM05367F12stomachMESH:D000230Adenocarcinomakidney
HM05367F12stomachMESH:D000230Adenocarcinomaeye
HM05367F12stomachMESH:D000230Adenocarcinomaadrenal gland
HM05367F12stomachMESH:D006258Head and Neck Neoplasmsthyroid
HM05367F12stomachMESH:D006258Head and Neck Neoplasmsskin
HM05367F12stomachMESH:D006258Head and Neck Neoplasmsparathyroid gland
HM05367F12stomachMESH:D006258Head and Neck Neoplasmslarynx
HM05367F12stomachMESH:D006258Head and Neck Neoplasmsear
HM05367F12stomachMESH:D006258Head and Neck Neoplasmsbrain
HM05367F12stomachMESH:D012004Rectal Neoplasmscolon
HM05367F12stomachMESH:D014846Vulvar Neoplasms
HM05367F12stomachMESH:D003072Cognition Disorders
HM05367F12stomachMESH:D017119Porphyria Cutanea Tardaskin
HM05367F12stomachMESH:D018248Adenoma, Liver Cell
HM05367F12stomachOMIM:610618ANGIOEDEMA, HEREDITARY, TYPE III
HM05367F12stomachMESH:D006331Heart Diseasesheart
HM05367F12stomachMESH:D006973Hypertensionlung
HM05367F12stomachMESH:D006973Hypertensionheart
HM05367F12stomachMESH:D006973Hypertensionblood vessel
HM05367F12stomachMESH:D014605Uveitiseye
HM05367F12stomachMESH:D002276Carcinoid Tumor
HM05367F12stomachMESH:D012878Skin Neoplasms
HM05367F12stomachMESH:D014564Urogenital Abnormalities
HM05367F12stomachMESH:D003882Dermatomyositisskin
HM05367F12stomachMESH:D005910Gliomabrain
HM05367F12stomachMESH:D005910Gliomaembryo
HM05367F12stomachMESH:D005910Gliomabrain
HM05367F12stomachMESH:D005910Gliomaspinal cord
HM05367F12stomachMESH:D005910Gliomabrain
HM05367F12stomachMESH:D003924Diabetes Mellitus, Type 2pancreas
HM05367F12stomachMESH:D004489Edema, Cardiac
HM05367F12stomachMESH:D015619Respiratory System Abnormalities
HM05367F12stomachMESH:D001714Bipolar Disorder
HM05367F12stomachMESH:D003110Colonic Neoplasmscolon
HM05367F12stomachMESH:D000740Anemiabone marrow
HM05367F12stomachMESH:D011471Prostatic Neoplasmsprostate
HM05367F12stomachMESH:D019282Wasting Syndrome
HM05367F12stomachMESH:D019584Hot Flashes
HM05367F12stomachMESH:D008106Liver Cirrhosis, Experimental
HM05367F12stomachMESH:D008175Lung Neoplasmslung
HM05367F12stomachMESH:D019465Craniofacial Abnormalities
HM05367F12stomachMESH:D005313Fetal Death
HM05367F12stomachMESH:D002295Carcinoma, Transitional Cell
HM05367F12stomachMESH:D003865Depressive Disorder, Major
HM05367F12stomachMESH:D004362Drug Toxicity
HM05367F12stomachMESH:D006529Hepatomegaly
HM05367F12stomachMESH:D009436Neural Tube Defects
HM05367F12stomachMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM05367F12stomachMESH:D015663Osteoporosis, Postmenopausal
HM05367F12stomachMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM05367F12stomachMESH:D006470Hemorrhage
HM05367F12stomachMESH:D010382Peliosis Hepatisliver
HM05367F12stomachMESH:D011693Purpurabone marrow
HM05367F12stomachMESH:D013959Thyroid Diseasesthyroid
HM05367F12stomachMESH:D002972Cleft Palate
HM05367F12stomachMESH:D006330Heart Defects, Congenital
HM05367F12stomachMESH:D000550Amblyopiabrain
HM05367F12stomachMESH:D000550Amblyopiabrain
HM05367F12stomachMESH:D006849Hydrocephalusbrain
HM05367F12stomachMESH:D052016Mucositis
HM05367F12stomachMESH:D001836Body Weight Changes
HM05367F12stomachMESH:D002318Cardiovascular Diseasesheart
HM05367F12stomachMESH:D002318Cardiovascular Diseasesbone marrow
HM05367F12stomachMESH:D002318Cardiovascular Diseasesblood vessel
HM05367F12stomachMESH:D006457Hemoglobinuria, Paroxysmal
HM05367F12stomachMESH:D007249Inflammation
HM05367F12stomachMESH:D007805Language Development Disorders
HM05367F12stomachMESH:D017202Myocardial Ischemiaheart
HM05367F12stomachMESH:D004487Edema
HM05367F12stomachMESH:D000544Alzheimer Diseasenerve
HM05367F12stomachMESH:D001008Anxiety Disorders
HM05367F12stomachMESH:D003550Cystic Fibrosis
HM05367F12stomachMESH:D020258Neurotoxicity Syndromes
HM05367F12stomachMESH:D014985Xerophthalmiaeye
HM05367F12stomachMESH:D000505Alopeciaskin
HM05367F12stomachMESH:D008881Migraine Disordersbrain
HM05367F12stomachMESH:D001749Urinary Bladder Neoplasmsureter
HM05367F12stomachMESH:D001749Urinary Bladder Neoplasmsbladder
HM05367F12stomachMESH:D003928Diabetic Nephropathies
HM05367F12stomachMESH:D007638Keratoconjunctivitis Siccaeye
HM05367F12stomachMESH:D006332Cardiomegaly
HM05367F12stomachMESH:D015179Colorectal Neoplasms
HM05367F12stomachMESH:D019310Pseudolymphoma
HM05367F12stomachMESH:D004832Epilepsy, Absencemuscle
HM05367F12stomachMESH:D009421Nervous System Malformations
HM05367F12stomachMESH:D010024Osteoporosisbone
HM05367F12stomachMESH:D013274Stomach Neoplasms
HM05367F12stomachMESH:D008114Liver Neoplasms, Experimental
HM05367F12stomachMESH:D002292Carcinoma, Renal Cellkidney
HM05367F12stomachMESH:D004827Epilepsymuscle
HM05367F12stomachMESH:D008664Metal Metabolism, Inborn Errorsskin
HM05367F12stomachMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM05367F12stomachMESH:D008664Metal Metabolism, Inborn Errorsliver
HM05367F12stomachMESH:D008664Metal Metabolism, Inborn Errorskidney
HM05367F12stomachMESH:D010190Pancreatic Neoplasmspancreas
HM05367F12stomachMESH:D005355Fibrosis
HM05367F12stomachMESH:D007889Leiomyomamuscle