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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06397TMCC3mouthMESH:D004827Epilepsymuscle
HM06397TMCC3mouthMESH:D001321Autistic Disorder
HM06397TMCC3mouthMESH:D004421Dystonia
HM06397TMCC3mouthMESH:D015428Myocardial Reperfusion Injury
HM06397TMCC3mouthMESH:D000015Abnormalities, Multiple
HM06397TMCC3mouthMESH:D009369Neoplasmsspleen
HM06397TMCC3mouthMESH:D009369Neoplasmsbone marrow
HM06397TMCC3mouthMESH:D019310Pseudolymphoma
HM06397TMCC3mouthMESH:D008103Liver Cirrhosisliver
HM06397TMCC3mouthMESH:D009135Muscular Diseasesmuscle
HM06397TMCC3mouthMESH:D004487Edema
HM06397TMCC3mouthMESH:D014178Translocation, Genetic
HM06397TMCC3mouthMESH:D004832Epilepsy, Absencemuscle
HM06397TMCC3mouthMESH:D001714Bipolar Disorder
HM06397TMCC3mouthMESH:D001943Breast Neoplasmsbreast
HM06397TMCC3mouthMESH:D003876Dermatitis, Atopicskin
HM06397TMCC3mouthMESH:D056486Drug-Induced Liver Injury
HM06397TMCC3mouthMESH:D015427Reperfusion Injury
HM06397TMCC3mouthMESH:D006849Hydrocephalusbrain
HM06397TMCC3mouthMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM06397TMCC3mouthMESH:D004831Epilepsies, Myoclonicmuscle
HM06397TMCC3mouthMESH:D005234Fatty Liver
HM06397TMCC3mouthMESH:D008113Liver Neoplasms
HM06397TMCC3mouthMESH:D008113Liver Neoplasms
HM06397TMCC3mouthMESH:D009139Musculoskeletal Abnormalities
HM06397TMCC3mouthMESH:D019465Craniofacial Abnormalities
HM06397TMCC3mouthMESH:D007249Inflammation
HM06397TMCC3mouthMESH:D012559Schizophrenia
HM06397TMCC3mouthMESH:D008106Liver Cirrhosis, Experimental
HM06397TMCC3mouthMESH:D050171Dyslipidemias
HM06397TMCC3mouthMESH:D002779Cholestasisliver
HM06397TMCC3mouthMESH:D017449Dermatitis, Allergic Contactskin
HM06397TMCC3mouthMESH:D000550Amblyopiabrain
HM06397TMCC3mouthMESH:D000550Amblyopiabrain
HM06397TMCC3mouthMESH:D016135Spinal Dysraphismspinal cord
HM06397TMCC3mouthMESH:D014564Urogenital Abnormalities
HM06397TMCC3mouthMESH:D018248Adenoma, Liver Cell
HM06397TMCC3mouthMESH:D020194Unverricht-Lundborg Syndromemuscle
HM06397TMCC3mouthMESH:D000014Abnormalities, Drug-Induced
HM06397TMCC3mouthMESH:D017563Lung Diseases, Interstitiallung
HM06397TMCC3mouthMESH:D007333Insulin Resistance
HM06397TMCC3mouthMESH:D009203Myocardial Infarctionheart
HM06397TMCC3mouthMESH:D008881Migraine Disordersbrain
HM06397TMCC3mouthMESH:D009436Neural Tube Defects
HM06397TMCC3mouthMESH:D005317Fetal Growth Retardation
HM06397TMCC3mouthMESH:D006333Heart Failureheart
HM06397TMCC3mouthMESH:D005355Fibrosis
HM06397TMCC3mouthMESH:D012640Seizuresmuscle
HM06397TMCC3mouthMESH:D001161Arteriosclerosisblood vessel
HM06397TMCC3mouthMESH:D005315Fetal Diseases
HM06397TMCC3mouthMESH:D006529Hepatomegaly
HM06397TMCC3mouthMESH:D009765Obesity
HM06397TMCC3mouthMESH:D055371Acute Lung Injury
HM06397TMCC3mouthMESH:D001848Bone Diseases, Developmental
HM06397TMCC3mouthMESH:D009190Myelodysplastic Syndromes
HM06397TMCC3mouthMESH:D012208Rhabdomyosarcomarectum
HM06397TMCC3mouthMESH:D012208Rhabdomyosarcomaprostate
HM06397TMCC3mouthMESH:D012208Rhabdomyosarcomamuscle
HM06397TMCC3mouthMESH:D013226Status Epilepticusmuscle
HM06397TMCC3mouthMESH:D013226Status Epilepticusmuscle
HM06397TMCC3mouthMESH:D013226Status Epilepticusmuscle
HM06397TMCC3mouthMESH:D001778Blood Coagulation Disordersbone marrow
HM06397TMCC3mouthMESH:D001008Anxiety Disorders
HM06397TMCC3mouthMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM06397TMCC3mouthMESH:D004828Epilepsies, Partialmuscle
HM06397TMCC3mouthMESH:D017029Epilepsy, Complex Partialmuscle
HM06397TMCC3mouthMESH:D006943Hyperglycemia