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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01826PFN1amnionMESH:D001836Body Weight Changes
HM01826PFN1amnionMESH:D002822Choriocarcinomabrain
HM01826PFN1amnionMESH:D015428Myocardial Reperfusion Injury
HM01826PFN1amnionMESH:D011625Pterygiumeye
HM01826PFN1amnionMESH:D012208Rhabdomyosarcomarectum
HM01826PFN1amnionMESH:D012208Rhabdomyosarcomaprostate
HM01826PFN1amnionMESH:D012208Rhabdomyosarcomamuscle
HM01826PFN1amnionMESH:D007569Jaw Abnormalities
HM01826PFN1amnionMESH:D017563Lung Diseases, Interstitiallung
HM01826PFN1amnionMESH:D002252Carbon Tetrachloride Poisoning
HM01826PFN1amnionMESH:D004832Epilepsy, Absencemuscle
HM01826PFN1amnionMESH:D055371Acute Lung Injury
HM01826PFN1amnionMESH:D008527Medulloblastomaembryo
HM01826PFN1amnionMESH:D009135Muscular Diseasesmuscle
HM01826PFN1amnionMESH:D016584Panic Disorder
HM01826PFN1amnionMESH:D015427Reperfusion Injury
HM01826PFN1amnionMESH:D004362Drug Toxicity
HM01826PFN1amnionMESH:D004714Endometrial Hyperplasia
HM01826PFN1amnionMESH:D014564Urogenital Abnormalities
HM01826PFN1amnionMESH:D021441Carcinoma, Pancreatic Ductal
HM01826PFN1amnionMESH:D007674Kidney Diseasesureter
HM01826PFN1amnionMESH:D007674Kidney Diseasespituitary
HM01826PFN1amnionMESH:D007674Kidney Diseaseskidney
HM01826PFN1amnionMESH:D008546Melanoma, Experimental
HM01826PFN1amnionMESH:D002779Cholestasisliver
HM01826PFN1amnionMESH:D020191Myoclonic Epilepsies, Progressivenerve
HM01826PFN1amnionMESH:D020191Myoclonic Epilepsies, Progressivemuscle
HM01826PFN1amnionMESH:D010954Plasmacytoma
HM01826PFN1amnionMESH:D001249Asthmalung
HM01826PFN1amnionMESH:D013964Thyroid Neoplasmsthyroid
HM01826PFN1amnionMESH:D014820Vitiligobone marrow
HM01826PFN1amnionMESH:D000152Acne Vulgaris
HM01826PFN1amnionMESH:D006330Heart Defects, Congenital
HM01826PFN1amnionMESH:D010190Pancreatic Neoplasmspancreas
HM01826PFN1amnionMESH:D012878Skin Neoplasms
HM01826PFN1amnionMESH:D019282Wasting Syndrome
HM01826PFN1amnionMESH:D001169Arthritis, Experimental
HM01826PFN1amnionMESH:D001848Bone Diseases, Developmental
HM01826PFN1amnionMESH:D017114Liver Failure, Acute
HM01826PFN1amnionMESH:D020521Strokeblood vessel
HM01826PFN1amnionMESH:D003294Seizures, Febrile
HM01826PFN1amnionMESH:D000743Anemia, Hemolytickidney
HM01826PFN1amnionMESH:D000743Anemia, Hemolyticbone marrow
HM01826PFN1amnionMESH:D018290Cervical Intraepithelial Neoplasia
HM01826PFN1amnionMESH:D008679Metaplasia
HM01826PFN1amnionMESH:D013274Stomach Neoplasms
HM01826PFN1amnionMESH:D006849Hydrocephalusbrain
HM01826PFN1amnionMESH:D006930Hyperalgesia
HM01826PFN1amnionMESH:D002386Cataractpancreas
HM01826PFN1amnionMESH:D002386Cataracteye
HM01826PFN1amnionMESH:D020078Neurogenic Inflammation
HM01826PFN1amnionMESH:D010051Ovarian Neoplasmsuterus
HM01826PFN1amnionMESH:D010051Ovarian Neoplasms
HM01826PFN1amnionMESH:D012559Schizophrenia
HM01826PFN1amnionMESH:D002294Carcinoma, Squamous Celllung
HM01826PFN1amnionMESH:D002294Carcinoma, Squamous Cellliver
HM01826PFN1amnionMESH:D002294Carcinoma, Squamous Celllarynx
HM01826PFN1amnionMESH:D002294Carcinoma, Squamous Cellkidney
HM01826PFN1amnionMESH:D002294Carcinoma, Squamous Celleye
HM01826PFN1amnionMESH:D019584Hot Flashes
HM01826PFN1amnionMESH:D009062Mouth Neoplasms
HM01826PFN1amnionMESH:D009362Neoplasm Metastasis
HM01826PFN1amnionMESH:D015663Osteoporosis, Postmenopausal
HM01826PFN1amnionMESH:D001714Bipolar Disorder
HM01826PFN1amnionMESH:D019465Craniofacial Abnormalities
HM01826PFN1amnionMESH:D007247Infertility, Female
HM01826PFN1amnionMESH:D000230Adenocarcinoma
HM01826PFN1amnionMESH:D000230Adenocarcinomauterus
HM01826PFN1amnionMESH:D000230Adenocarcinoma
HM01826PFN1amnionMESH:D000230Adenocarcinoma
HM01826PFN1amnionMESH:D000230Adenocarcinomauterus
HM01826PFN1amnionMESH:D000230Adenocarcinomathyroid
HM01826PFN1amnionMESH:D000230Adenocarcinomaskin
HM01826PFN1amnionMESH:D000230Adenocarcinomaparathyroid gland
HM01826PFN1amnionMESH:D000230Adenocarcinomaliver
HM01826PFN1amnionMESH:D000230Adenocarcinomakidney
HM01826PFN1amnionMESH:D000230Adenocarcinomaeye
HM01826PFN1amnionMESH:D000230Adenocarcinomaadrenal gland
HM01826PFN1amnionMESH:D003110Colonic Neoplasmscolon
HM01826PFN1amnionMESH:D000013Congenital Abnormalities
HM01826PFN1amnionMESH:D005234Fatty Liver
HM01826PFN1amnionMESH:D010024Osteoporosisbone
HM01826PFN1amnionMESH:D011297Prenatal Exposure Delayed Effects
HM01826PFN1amnionMESH:D014062Tongue Neoplasms
HM01826PFN1amnionMESH:D056486Drug-Induced Liver Injury
HM01826PFN1amnionMESH:D007938Leukemiaspleen
HM01826PFN1amnionMESH:D007938Leukemiabone marrow
HM01826PFN1amnionMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM01826PFN1amnionMESH:D009396Wilms Tumorkidney
HM01826PFN1amnionMESH:D009396Wilms Tumorcervix
HM01826PFN1amnionMESH:D008106Liver Cirrhosis, Experimental
HM01826PFN1amnionMESH:D008107Liver Diseasesskin
HM01826PFN1amnionMESH:D008107Liver Diseasesmuscle
HM01826PFN1amnionMESH:D008107Liver Diseaseslung
HM01826PFN1amnionMESH:D008107Liver Diseasesliver
HM01826PFN1amnionMESH:D014376Tuberculosis
HM01826PFN1amnionMESH:D001749Urinary Bladder Neoplasmsureter
HM01826PFN1amnionMESH:D001749Urinary Bladder Neoplasmsbladder
HM01826PFN1amnionMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM01826PFN1amnionMESH:D006317Hearing Loss, Noise-Induced
HM01826PFN1amnionMESH:D014594Uterine Neoplasmscervix
HM01826PFN1amnionMESH:D014594Uterine Neoplasms
HM01826PFN1amnionMESH:D017202Myocardial Ischemiaheart
HM01826PFN1amnionMESH:D001778Blood Coagulation Disordersbone marrow
HM01826PFN1amnionMESH:D006332Cardiomegaly
HM01826PFN1amnionMESH:D008654Mesotheliomabone
HM01826PFN1amnionMESH:D010146Pain
HM01826PFN1amnionMESH:D018281Cholangiocarcinomaliver
HM01826PFN1amnionMESH:D015473Leukemia, Promyelocytic, Acute
HM01826PFN1amnionMESH:D014581Urticariaskin
HM01826PFN1amnionMESH:D004938Esophageal Neoplasms
HM01826PFN1amnionMESH:D009765Obesity
HM01826PFN1amnionMESH:D007410Intestinal Diseasessmall intestine
HM01826PFN1amnionMESH:D007410Intestinal Diseasesrectum
HM01826PFN1amnionMESH:D007410Intestinal Diseasescolon
HM01826PFN1amnionMESH:D007410Intestinal Diseasesblood vessel
HM01826PFN1amnionMESH:D007951Leukemia, Myeloidbone marrow
HM01826PFN1amnionMESH:D003921Diabetes Mellitus, Experimental
HM01826PFN1amnionMESH:D007676Kidney Failure, Chronickidney
HM01826PFN1amnionMESH:D008171Lung Diseases
HM01826PFN1amnionMESH:D010538Peritonitis
HM01826PFN1amnionMESH:D011471Prostatic Neoplasmsprostate
HM01826PFN1amnionMESH:D001471Barrett Esophagusesophagus
HM01826PFN1amnionMESH:D001997Bronchopulmonary Dysplasialung
HM01826PFN1amnionMESH:D004487Edema
HM01826PFN1amnionMESH:D005909Glioblastomabone
HM01826PFN1amnionMESH:D005909Glioblastomabrain
HM01826PFN1amnionMESH:D005909Glioblastomabone
HM01826PFN1amnionMESH:D008113Liver Neoplasms
HM01826PFN1amnionMESH:D008113Liver Neoplasms
HM01826PFN1amnionMESH:D009421Nervous System Malformations
HM01826PFN1amnionMESH:D000015Abnormalities, Multiple
HM01826PFN1amnionMESH:D000550Amblyopiabrain
HM01826PFN1amnionMESH:D000550Amblyopiabrain
HM01826PFN1amnionMESH:D006869Hydronephrosiskidney
HM01826PFN1amnionMESH:D007249Inflammation
HM01826PFN1amnionMESH:D007627Keloid
HM01826PFN1amnionMESH:D000236Adenomapancreas
HM01826PFN1amnionMESH:D000236Adenomaliver
HM01826PFN1amnionMESH:D000236Adenomakidney
HM01826PFN1amnionMESH:D000236Adenoma
HM01826PFN1amnionMESH:D000236Adenoma
HM01826PFN1amnionMESH:D000236Adenoma
HM01826PFN1amnionMESH:D000236Adenoma
HM01826PFN1amnionMESH:D005910Gliomabrain
HM01826PFN1amnionMESH:D005910Gliomaembryo
HM01826PFN1amnionMESH:D005910Gliomabrain
HM01826PFN1amnionMESH:D005910Gliomaspinal cord
HM01826PFN1amnionMESH:D005910Gliomabrain
HM01826PFN1amnionMESH:D017681Hypereosinophilic Syndrome
HM01826PFN1amnionMESH:D004828Epilepsies, Partialmuscle
HM01826PFN1amnionMESH:D005124Eye Abnormalities
HM01826PFN1amnionMESH:D006470Hemorrhage
HM01826PFN1amnionMESH:D003092Colitis
HM01826PFN1amnionMESH:D007251Influenza, Human
HM01826PFN1amnionMESH:D014604Uveal Neoplasmseye
HM01826PFN1amnionMESH:D011507Proteinuriakidney
HM01826PFN1amnionMESH:D012554Schistosomiasis japonica
HM01826PFN1amnionMESH:D008881Migraine Disordersbrain
HM01826PFN1amnionMESH:D006943Hyperglycemia
HM01826PFN1amnionMESH:D013226Status Epilepticusmuscle
HM01826PFN1amnionMESH:D013226Status Epilepticusmuscle
HM01826PFN1amnionMESH:D013226Status Epilepticusmuscle
HM01826PFN1amnionMESH:D000740Anemiabone marrow
HM01826PFN1amnionMESH:D008591Meningomyelocele
HM01826PFN1amnionMESH:D009203Myocardial Infarctionheart
HM01826PFN1amnionMESH:D010018Osteomalaciabone
HM01826PFN1amnionMESH:D000544Alzheimer Diseasenerve
HM01826PFN1amnionMESH:D007021Hypospadias
HM01826PFN1amnionMESH:D010382Peliosis Hepatisliver
HM01826PFN1amnionMESH:D054079Vascular Malformations
HM01826PFN1amnionMESH:D004421Dystonia
HM01826PFN1amnionMESH:D001943Breast Neoplasmsbreast
HM01826PFN1amnionMESH:D019636Neurodegenerative Diseasesnerve
HM01826PFN1amnionMESH:D004831Epilepsies, Myoclonicmuscle
HM01826PFN1amnionMESH:D005355Fibrosis
HM01826PFN1amnionMESH:D012640Seizuresmuscle
HM01826PFN1amnionMESH:D002493Central Nervous System Diseasesspinal cord
HM01826PFN1amnionMESH:D002493Central Nervous System Diseasesskin
HM01826PFN1amnionMESH:D002493Central Nervous System Diseasesnerve
HM01826PFN1amnionMESH:D002493Central Nervous System Diseasesmuscle
HM01826PFN1amnionMESH:D002493Central Nervous System Diseaseseye
HM01826PFN1amnionMESH:D002493Central Nervous System Diseasesbrain
HM01826PFN1amnionMESH:D017029Epilepsy, Complex Partialmuscle
HM01826PFN1amnionMESH:D006333Heart Failureheart
HM01826PFN1amnionMESH:D009436Neural Tube Defects
HM01826PFN1amnionMESH:D007248Infertility, Male
HM01826PFN1amnionMESH:D015619Respiratory System Abnormalities
HM01826PFN1amnionMESH:D006528Carcinoma, Hepatocellularliver
HM01826PFN1amnionMESH:D017119Porphyria Cutanea Tardaskin
HM01826PFN1amnionMESH:D011230Precancerous Conditions
HM01826PFN1amnionMESH:D000505Alopeciaskin
HM01826PFN1amnionMESH:D000799Angioedemaskin
HM01826PFN1amnionMESH:D002318Cardiovascular Diseasesheart
HM01826PFN1amnionMESH:D002318Cardiovascular Diseasesbone marrow
HM01826PFN1amnionMESH:D002318Cardiovascular Diseasesblood vessel
HM01826PFN1amnionMESH:D004827Epilepsymuscle
HM01826PFN1amnionMESH:D006529Hepatomegaly
HM01826PFN1amnionMESH:D009369Neoplasmsspleen
HM01826PFN1amnionMESH:D009369Neoplasmsbone marrow
HM01826PFN1amnionMESH:D000014Abnormalities, Drug-Induced
HM01826PFN1amnionMESH:D020246Venous Thrombosis
HM01826PFN1amnionMESH:D018248Adenoma, Liver Cell
HM01826PFN1amnionMESH:D002105Cadmium Poisoning
HM01826PFN1amnionMESH:D005313Fetal Death
HM01826PFN1amnionMESH:D008545Melanomaeye
HM01826PFN1amnionMESH:D008545Melanomacervix
HM01826PFN1amnionMESH:D008545Melanomabone
HM01826PFN1amnionMESH:D001008Anxiety Disorders
HM01826PFN1amnionMESH:D003876Dermatitis, Atopicskin
HM01826PFN1amnionMESH:D004489Edema, Cardiac
HM01826PFN1amnionMESH:D002100Cachexia
HM01826PFN1amnionMESH:D002972Cleft Palate
HM01826PFN1amnionMESH:D007333Insulin Resistance
HM01826PFN1amnionMESH:D008175Lung Neoplasmslung
HM01826PFN1amnionMESH:D013959Thyroid Diseasesthyroid
HM01826PFN1amnionMESH:D003924Diabetes Mellitus, Type 2pancreas
HM01826PFN1amnionMESH:D005315Fetal Diseases
HM01826PFN1amnionMESH:D008325Mammary Neoplasms, Experimental
HM01826PFN1amnionMESH:D016535Bronchial Hyperreactivity
HM01826PFN1amnionMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM01826PFN1amnionMESH:D009190Myelodysplastic Syndromes
HM01826PFN1amnionMESH:D001321Autistic Disorder
HM01826PFN1amnionMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM01826PFN1amnionMESH:D016889Endometrial Neoplasmsuterus
HM01826PFN1amnionMESH:D006548Hernia, Diaphragmatic
HM01826PFN1amnionMESH:D002583Uterine Cervical Neoplasmscervix
HM01826PFN1amnionMESH:D002277Carcinoma
HM01826PFN1amnionMESH:D016135Spinal Dysraphismspinal cord
HM01826PFN1amnionMESH:D001161Arteriosclerosisblood vessel
HM01826PFN1amnionMESH:D018236Carcinoma, Embryonal
HM01826PFN1amnionMESH:D006258Head and Neck Neoplasmsthyroid
HM01826PFN1amnionMESH:D006258Head and Neck Neoplasmsskin
HM01826PFN1amnionMESH:D006258Head and Neck Neoplasmsparathyroid gland
HM01826PFN1amnionMESH:D006258Head and Neck Neoplasmslarynx
HM01826PFN1amnionMESH:D006258Head and Neck Neoplasmsear
HM01826PFN1amnionMESH:D006258Head and Neck Neoplasmsbrain
HM01826PFN1amnionMESH:D011537Pruritus
HM01826PFN1amnionMESH:D013927Thrombosis
HM01826PFN1amnionMESH:D006973Hypertensionlung
HM01826PFN1amnionMESH:D006973Hypertensionheart
HM01826PFN1amnionMESH:D006973Hypertensionblood vessel
HM01826PFN1amnionMESH:D020194Unverricht-Lundborg Syndromemuscle
HM01826PFN1amnionMESH:D011014Pneumonialung
HM01826PFN1amnionMESH:D019851Thrombophiliabone marrow
HM01826PFN1amnionMESH:D015179Colorectal Neoplasms
HM01826PFN1amnionMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM01826PFN1amnionMESH:D001260Ataxia Telangiectasia
HM01826PFN1amnionMESH:D013088Spermatocele
HM01826PFN1amnionMESH:D001172Arthritis, Rheumatoidbone
HM01826PFN1amnionMESH:D001327Autoimmune Diseasesskin
HM01826PFN1amnionMESH:D001327Autoimmune Diseasesparathyroid gland
HM01826PFN1amnionMESH:D001327Autoimmune Diseaseslung
HM01826PFN1amnionMESH:D001327Autoimmune Diseaseseye
HM01826PFN1amnionMESH:D001327Autoimmune Diseasesbone marrow
HM01826PFN1amnionMESH:D001932Brain Neoplasmsbrain
HM01826PFN1amnionMESH:D017880Limb Deformities, Congenital
HM01826PFN1amnionMESH:D008114Liver Neoplasms, Experimental
HM01826PFN1amnionMESH:D009139Musculoskeletal Abnormalities
HM01826PFN1amnionMESH:D019310Pseudolymphoma
HM01826PFN1amnionMESH:D014178Translocation, Genetic
HM01826PFN1amnionMESH:D005317Fetal Growth Retardation