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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05829CDC42EP5stomachMESH:D000014Abnormalities, Drug-Induced
HM05829CDC42EP5stomachMESH:D004831Epilepsies, Myoclonicmuscle
HM05829CDC42EP5stomachMESH:D014594Uterine Neoplasmscervix
HM05829CDC42EP5stomachMESH:D014594Uterine Neoplasms
HM05829CDC42EP5stomachMESH:D012208Rhabdomyosarcomarectum
HM05829CDC42EP5stomachMESH:D012208Rhabdomyosarcomaprostate
HM05829CDC42EP5stomachMESH:D012208Rhabdomyosarcomamuscle
HM05829CDC42EP5stomachMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM05829CDC42EP5stomachMESH:D007249Inflammation
HM05829CDC42EP5stomachMESH:D020194Unverricht-Lundborg Syndromemuscle
HM05829CDC42EP5stomachMESH:D004828Epilepsies, Partialmuscle
HM05829CDC42EP5stomachMESH:D013927Thrombosis
HM05829CDC42EP5stomachMESH:D006973Hypertensionlung
HM05829CDC42EP5stomachMESH:D006973Hypertensionheart
HM05829CDC42EP5stomachMESH:D006973Hypertensionblood vessel
HM05829CDC42EP5stomachMESH:D014178Translocation, Genetic
HM05829CDC42EP5stomachMESH:D012878Skin Neoplasms
HM05829CDC42EP5stomachMESH:D005234Fatty Liver
HM05829CDC42EP5stomachMESH:D003294Seizures, Febrile
HM05829CDC42EP5stomachMESH:D020246Venous Thrombosis
HM05829CDC42EP5stomachMESH:D002493Central Nervous System Diseasesspinal cord
HM05829CDC42EP5stomachMESH:D002493Central Nervous System Diseasesskin
HM05829CDC42EP5stomachMESH:D002493Central Nervous System Diseasesnerve
HM05829CDC42EP5stomachMESH:D002493Central Nervous System Diseasesmuscle
HM05829CDC42EP5stomachMESH:D002493Central Nervous System Diseaseseye
HM05829CDC42EP5stomachMESH:D002493Central Nervous System Diseasesbrain
HM05829CDC42EP5stomachMESH:D005315Fetal Diseases
HM05829CDC42EP5stomachMESH:D001008Anxiety Disorders
HM05829CDC42EP5stomachMESH:D009436Neural Tube Defects
HM05829CDC42EP5stomachMESH:D013959Thyroid Diseasesthyroid
HM05829CDC42EP5stomachMESH:D000013Congenital Abnormalities
HM05829CDC42EP5stomachMESH:D006332Cardiomegaly
HM05829CDC42EP5stomachMESH:D005317Fetal Growth Retardation
HM05829CDC42EP5stomachMESH:D000015Abnormalities, Multiple
HM05829CDC42EP5stomachMESH:D006529Hepatomegaly
HM05829CDC42EP5stomachMESH:D004362Drug Toxicity
HM05829CDC42EP5stomachMESH:D001714Bipolar Disorder
HM05829CDC42EP5stomachMESH:D002277Carcinoma
HM05829CDC42EP5stomachMESH:D010190Pancreatic Neoplasmspancreas
HM05829CDC42EP5stomachMESH:D000152Acne Vulgaris
HM05829CDC42EP5stomachMESH:D000230Adenocarcinoma
HM05829CDC42EP5stomachMESH:D000230Adenocarcinomauterus
HM05829CDC42EP5stomachMESH:D000230Adenocarcinoma
HM05829CDC42EP5stomachMESH:D000230Adenocarcinoma
HM05829CDC42EP5stomachMESH:D000230Adenocarcinomauterus
HM05829CDC42EP5stomachMESH:D000230Adenocarcinomathyroid
HM05829CDC42EP5stomachMESH:D000230Adenocarcinomaskin
HM05829CDC42EP5stomachMESH:D000230Adenocarcinomaparathyroid gland
HM05829CDC42EP5stomachMESH:D000230Adenocarcinomaliver
HM05829CDC42EP5stomachMESH:D000230Adenocarcinomakidney
HM05829CDC42EP5stomachMESH:D000230Adenocarcinomaeye
HM05829CDC42EP5stomachMESH:D000230Adenocarcinomaadrenal gland
HM05829CDC42EP5stomachMESH:D011230Precancerous Conditions
HM05829CDC42EP5stomachMESH:D013088Spermatocele
HM05829CDC42EP5stomachMESH:D008114Liver Neoplasms, Experimental
HM05829CDC42EP5stomachMESH:D019310Pseudolymphoma
HM05829CDC42EP5stomachMESH:D000740Anemiabone marrow
HM05829CDC42EP5stomachMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM05829CDC42EP5stomachMESH:D004827Epilepsymuscle
HM05829CDC42EP5stomachMESH:D018248Adenoma, Liver Cell
HM05829CDC42EP5stomachMESH:D019282Wasting Syndrome
HM05829CDC42EP5stomachMESH:D002779Cholestasisliver
HM05829CDC42EP5stomachMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM05829CDC42EP5stomachMESH:D001169Arthritis, Experimental
HM05829CDC42EP5stomachMESH:D001848Bone Diseases, Developmental
HM05829CDC42EP5stomachMESH:D008881Migraine Disordersbrain
HM05829CDC42EP5stomachMESH:D006330Heart Defects, Congenital
HM05829CDC42EP5stomachMESH:D012559Schizophrenia
HM05829CDC42EP5stomachMESH:D006528Carcinoma, Hepatocellularliver
HM05829CDC42EP5stomachMESH:D002972Cleft Palate
HM05829CDC42EP5stomachMESH:D017202Myocardial Ischemiaheart
HM05829CDC42EP5stomachMESH:D001161Arteriosclerosisblood vessel
HM05829CDC42EP5stomachMESH:D001321Autistic Disorder
HM05829CDC42EP5stomachMESH:D008107Liver Diseasesskin
HM05829CDC42EP5stomachMESH:D008107Liver Diseasesmuscle
HM05829CDC42EP5stomachMESH:D008107Liver Diseaseslung
HM05829CDC42EP5stomachMESH:D008107Liver Diseasesliver
HM05829CDC42EP5stomachMESH:D016135Spinal Dysraphismspinal cord
HM05829CDC42EP5stomachMESH:D001778Blood Coagulation Disordersbone marrow
HM05829CDC42EP5stomachMESH:D008106Liver Cirrhosis, Experimental
HM05829CDC42EP5stomachMESH:D009190Myelodysplastic Syndromes
HM05829CDC42EP5stomachMESH:D020191Myoclonic Epilepsies, Progressivenerve
HM05829CDC42EP5stomachMESH:D020191Myoclonic Epilepsies, Progressivemuscle
HM05829CDC42EP5stomachMESH:D014564Urogenital Abnormalities
HM05829CDC42EP5stomachMESH:D001943Breast Neoplasmsbreast
HM05829CDC42EP5stomachMESH:D010382Peliosis Hepatisliver
HM05829CDC42EP5stomachMESH:D018281Cholangiocarcinomaliver
HM05829CDC42EP5stomachMESH:D003924Diabetes Mellitus, Type 2pancreas
HM05829CDC42EP5stomachMESH:D011537Pruritus
HM05829CDC42EP5stomachMESH:D017029Epilepsy, Complex Partialmuscle
HM05829CDC42EP5stomachMESH:D006470Hemorrhage
HM05829CDC42EP5stomachMESH:D009421Nervous System Malformations
HM05829CDC42EP5stomachMESH:D001836Body Weight Changes
HM05829CDC42EP5stomachMESH:D007569Jaw Abnormalities
HM05829CDC42EP5stomachMESH:D007248Infertility, Male
HM05829CDC42EP5stomachMESH:D012640Seizuresmuscle
HM05829CDC42EP5stomachMESH:D010018Osteomalaciabone
HM05829CDC42EP5stomachMESH:D054079Vascular Malformations
HM05829CDC42EP5stomachMESH:D006869Hydronephrosiskidney
HM05829CDC42EP5stomachMESH:D005313Fetal Death
HM05829CDC42EP5stomachMESH:D013226Status Epilepticusmuscle
HM05829CDC42EP5stomachMESH:D013226Status Epilepticusmuscle
HM05829CDC42EP5stomachMESH:D013226Status Epilepticusmuscle
HM05829CDC42EP5stomachMESH:D004487Edema
HM05829CDC42EP5stomachMESH:D004832Epilepsy, Absencemuscle
HM05829CDC42EP5stomachMESH:D017563Lung Diseases, Interstitiallung
HM05829CDC42EP5stomachMESH:D009139Musculoskeletal Abnormalities
HM05829CDC42EP5stomachMESH:D011297Prenatal Exposure Delayed Effects
HM05829CDC42EP5stomachMESH:D005124Eye Abnormalities
HM05829CDC42EP5stomachMESH:D008113Liver Neoplasms
HM05829CDC42EP5stomachMESH:D008113Liver Neoplasms
HM05829CDC42EP5stomachMESH:D008175Lung Neoplasmslung
HM05829CDC42EP5stomachMESH:D016584Panic Disorder
HM05829CDC42EP5stomachMESH:D017119Porphyria Cutanea Tardaskin
HM05829CDC42EP5stomachMESH:D015619Respiratory System Abnormalities
HM05829CDC42EP5stomachMESH:D056486Drug-Induced Liver Injury
HM05829CDC42EP5stomachMESH:D004489Edema, Cardiac
HM05829CDC42EP5stomachMESH:D005355Fibrosis
HM05829CDC42EP5stomachMESH:D007247Infertility, Female
HM05829CDC42EP5stomachMESH:D007021Hypospadias
HM05829CDC42EP5stomachMESH:D019851Thrombophiliabone marrow
HM05829CDC42EP5stomachMESH:D000550Amblyopiabrain
HM05829CDC42EP5stomachMESH:D000550Amblyopiabrain
HM05829CDC42EP5stomachMESH:D004421Dystonia
HM05829CDC42EP5stomachMESH:D006849Hydrocephalusbrain
HM05829CDC42EP5stomachMESH:D019465Craniofacial Abnormalities