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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04071CPVLpharynxMESH:D008113Liver Neoplasms
HM04071CPVLpharynxMESH:D008113Liver Neoplasms
HM04071CPVLpharynxMESH:D014652Vascular Diseasesspinal cord
HM04071CPVLpharynxMESH:D014652Vascular Diseaseslung
HM04071CPVLpharynxMESH:D014652Vascular Diseasesliver
HM04071CPVLpharynxMESH:D014652Vascular Diseaseskidney
HM04071CPVLpharynxMESH:D014652Vascular Diseasesblood vessel
HM04071CPVLpharynxMESH:D006528Carcinoma, Hepatocellularliver
HM04071CPVLpharynxMESH:D009190Myelodysplastic Syndromes
HM04071CPVLpharynxMESH:D018281Cholangiocarcinomaliver
HM04071CPVLpharynxMESH:D004832Epilepsy, Absencemuscle
HM04071CPVLpharynxMESH:D008175Lung Neoplasmslung
HM04071CPVLpharynxMESH:D001749Urinary Bladder Neoplasmsureter
HM04071CPVLpharynxMESH:D001749Urinary Bladder Neoplasmsbladder
HM04071CPVLpharynxMESH:D001836Body Weight Changes
HM04071CPVLpharynxMESH:D005317Fetal Growth Retardation
HM04071CPVLpharynxMESH:D007674Kidney Diseasesureter
HM04071CPVLpharynxMESH:D007674Kidney Diseasespituitary
HM04071CPVLpharynxMESH:D007674Kidney Diseaseskidney
HM04071CPVLpharynxMESH:D020194Unverricht-Lundborg Syndromemuscle
HM04071CPVLpharynxMESH:D005234Fatty Liver
HM04071CPVLpharynxMESH:D004828Epilepsies, Partialmuscle
HM04071CPVLpharynxMESH:D006689Hodgkin Disease
HM04071CPVLpharynxMESH:D015619Respiratory System Abnormalities
HM04071CPVLpharynxMESH:D008171Lung Diseases
HM04071CPVLpharynxMESH:D009062Mouth Neoplasms
HM04071CPVLpharynxMESH:D016135Spinal Dysraphismspinal cord
HM04071CPVLpharynxMESH:D002294Carcinoma, Squamous Celllung
HM04071CPVLpharynxMESH:D002294Carcinoma, Squamous Cellliver
HM04071CPVLpharynxMESH:D002294Carcinoma, Squamous Celllarynx
HM04071CPVLpharynxMESH:D002294Carcinoma, Squamous Cellkidney
HM04071CPVLpharynxMESH:D002294Carcinoma, Squamous Celleye
HM04071CPVLpharynxMESH:D010051Ovarian Neoplasmsuterus
HM04071CPVLpharynxMESH:D010051Ovarian Neoplasms
HM04071CPVLpharynxMESH:D008114Liver Neoplasms, Experimental
HM04071CPVLpharynxMESH:D014178Translocation, Genetic
HM04071CPVLpharynxMESH:D001008Anxiety Disorders
HM04071CPVLpharynxMESH:D000015Abnormalities, Multiple
HM04071CPVLpharynxMESH:D019465Craniofacial Abnormalities
HM04071CPVLpharynxMESH:D012640Seizuresmuscle
HM04071CPVLpharynxMESH:D001778Blood Coagulation Disordersbone marrow
HM04071CPVLpharynxMESH:D004938Esophageal Neoplasms
HM04071CPVLpharynxMESH:D015451Leukemia, Lymphocytic, Chronic, B-Cellbone marrow
HM04071CPVLpharynxMESH:D000550Amblyopiabrain
HM04071CPVLpharynxMESH:D000550Amblyopiabrain
HM04071CPVLpharynxMESH:D007249Inflammation
HM04071CPVLpharynxMESH:D004487Edema
HM04071CPVLpharynxMESH:D004831Epilepsies, Myoclonicmuscle
HM04071CPVLpharynxMESH:D006331Heart Diseasesheart
HM04071CPVLpharynxMESH:D001848Bone Diseases, Developmental
HM04071CPVLpharynxMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM04071CPVLpharynxMESH:D013226Status Epilepticusmuscle
HM04071CPVLpharynxMESH:D013226Status Epilepticusmuscle
HM04071CPVLpharynxMESH:D013226Status Epilepticusmuscle
HM04071CPVLpharynxMESH:D004421Dystonia
HM04071CPVLpharynxMESH:D007248Infertility, Male
HM04071CPVLpharynxMESH:D017563Lung Diseases, Interstitiallung
HM04071CPVLpharynxMESH:D013959Thyroid Diseasesthyroid
HM04071CPVLpharynxMESH:D054079Vascular Malformations
HM04071CPVLpharynxMESH:D003921Diabetes Mellitus, Experimental
HM04071CPVLpharynxMESH:D017029Epilepsy, Complex Partialmuscle
HM04071CPVLpharynxMESH:D007569Jaw Abnormalities
HM04071CPVLpharynxMESH:D006332Cardiomegaly
HM04071CPVLpharynxMESH:D012208Rhabdomyosarcomarectum
HM04071CPVLpharynxMESH:D012208Rhabdomyosarcomaprostate
HM04071CPVLpharynxMESH:D012208Rhabdomyosarcomamuscle
HM04071CPVLpharynxMESH:D003924Diabetes Mellitus, Type 2pancreas
HM04071CPVLpharynxMESH:D005833Genital Neoplasms, Female
HM04071CPVLpharynxMESH:D002471Cell Transformation, Neoplastic
HM04071CPVLpharynxMESH:D000230Adenocarcinoma
HM04071CPVLpharynxMESH:D000230Adenocarcinomauterus
HM04071CPVLpharynxMESH:D000230Adenocarcinoma
HM04071CPVLpharynxMESH:D000230Adenocarcinoma
HM04071CPVLpharynxMESH:D000230Adenocarcinomauterus
HM04071CPVLpharynxMESH:D000230Adenocarcinomathyroid
HM04071CPVLpharynxMESH:D000230Adenocarcinomaskin
HM04071CPVLpharynxMESH:D000230Adenocarcinomaparathyroid gland
HM04071CPVLpharynxMESH:D000230Adenocarcinomaliver
HM04071CPVLpharynxMESH:D000230Adenocarcinomakidney
HM04071CPVLpharynxMESH:D000230Adenocarcinomaeye
HM04071CPVLpharynxMESH:D000230Adenocarcinomaadrenal gland
HM04071CPVLpharynxMESH:D018246Adrenocortical Adenoma
HM04071CPVLpharynxMESH:D005315Fetal Diseases
HM04071CPVLpharynxMESH:D001943Breast Neoplasmsbreast
HM04071CPVLpharynxMESH:D004489Edema, Cardiac
HM04071CPVLpharynxMESH:D000013Congenital Abnormalities
HM04071CPVLpharynxMESH:D006330Heart Defects, Congenital
HM04071CPVLpharynxMESH:D018248Adenoma, Liver Cell
HM04071CPVLpharynxMESH:D005355Fibrosis
HM04071CPVLpharynxMESH:D004362Drug Toxicity
HM04071CPVLpharynxMESH:D002277Carcinoma
HM04071CPVLpharynxMESH:D009436Neural Tube Defects
HM04071CPVLpharynxMESH:D006869Hydronephrosiskidney
HM04071CPVLpharynxMESH:D010382Peliosis Hepatisliver
HM04071CPVLpharynxMESH:D011471Prostatic Neoplasmsprostate
HM04071CPVLpharynxMESH:D012878Skin Neoplasms
HM04071CPVLpharynxMESH:D000310Adrenal Gland Neoplasmsadrenal gland
HM04071CPVLpharynxMESH:D000310Adrenal Gland Neoplasmsadrenal gland
HM04071CPVLpharynxMESH:D019310Pseudolymphoma
HM04071CPVLpharynxMESH:D006529Hepatomegaly
HM04071CPVLpharynxMESH:D008106Liver Cirrhosis, Experimental
HM04071CPVLpharynxMESH:D011297Prenatal Exposure Delayed Effects
HM04071CPVLpharynxMESH:D002583Uterine Cervical Neoplasmscervix
HM04071CPVLpharynxMESH:D005313Fetal Death
HM04071CPVLpharynxMESH:D008545Melanomaeye
HM04071CPVLpharynxMESH:D008545Melanomacervix
HM04071CPVLpharynxMESH:D008545Melanomabone
HM04071CPVLpharynxMESH:D004827Epilepsymuscle
HM04071CPVLpharynxMESH:D009139Musculoskeletal Abnormalities
HM04071CPVLpharynxMESH:D056486Drug-Induced Liver Injury
HM04071CPVLpharynxMESH:D000014Abnormalities, Drug-Induced
HM04071CPVLpharynxMESH:D001714Bipolar Disorder
HM04071CPVLpharynxMESH:D009374Neoplasms, Experimental
HM04071CPVLpharynxMESH:D008881Migraine Disordersbrain
HM04071CPVLpharynxMESH:D000740Anemiabone marrow
HM04071CPVLpharynxMESH:D006849Hydrocephalusbrain
HM04071CPVLpharynxMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM04071CPVLpharynxMESH:D005124Eye Abnormalities
HM04071CPVLpharynxMESH:D001321Autistic Disorder
HM04071CPVLpharynxMESH:D002972Cleft Palate
HM04071CPVLpharynxMESH:D009369Neoplasmsspleen
HM04071CPVLpharynxMESH:D009369Neoplasmsbone marrow
HM04071CPVLpharynxMESH:D009421Nervous System Malformations
HM04071CPVLpharynxMESH:D012559Schizophrenia
HM04071CPVLpharynxMESH:D006470Hemorrhage
HM04071CPVLpharynxMESH:D006973Hypertensionlung
HM04071CPVLpharynxMESH:D006973Hypertensionheart
HM04071CPVLpharynxMESH:D006973Hypertensionblood vessel
HM04071CPVLpharynxMESH:D017202Myocardial Ischemiaheart
HM04071CPVLpharynxMESH:D017119Porphyria Cutanea Tardaskin
HM04071CPVLpharynxMESH:D014564Urogenital Abnormalities
HM04071CPVLpharynxMESH:D019282Wasting Syndrome
HM04071CPVLpharynxMESH:D013274Stomach Neoplasms