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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01899CD1CthymusMESH:D004421Dystonia
HM01899CD1CthymusMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM01899CD1CthymusMESH:D009139Musculoskeletal Abnormalities
HM01899CD1CthymusMESH:D014564Urogenital Abnormalities
HM01899CD1CthymusMESH:D000015Abnormalities, Multiple
HM01899CD1CthymusMESH:D008881Migraine Disordersbrain
HM01899CD1CthymusMESH:D012208Rhabdomyosarcomarectum
HM01899CD1CthymusMESH:D012208Rhabdomyosarcomaprostate
HM01899CD1CthymusMESH:D012208Rhabdomyosarcomamuscle
HM01899CD1CthymusMESH:D004828Epilepsies, Partialmuscle
HM01899CD1CthymusMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM01899CD1CthymusMESH:D000163Acquired Immunodeficiency Syndrome
HM01899CD1CthymusMESH:D012640Seizuresmuscle
HM01899CD1CthymusMESH:D019465Craniofacial Abnormalities
HM01899CD1CthymusMESH:D004832Epilepsy, Absencemuscle
HM01899CD1CthymusMESH:D008106Liver Cirrhosis, Experimental
HM01899CD1CthymusMESH:D007251Influenza, Human
HM01899CD1CthymusMESH:D008171Lung Diseases
HM01899CD1CthymusMESH:D013274Stomach Neoplasms
HM01899CD1CthymusMESH:D016135Spinal Dysraphismspinal cord
HM01899CD1CthymusMESH:D056486Drug-Induced Liver Injury
HM01899CD1CthymusMESH:D019584Hot Flashes
HM01899CD1CthymusMESH:D001321Autistic Disorder
HM01899CD1CthymusMESH:D004827Epilepsymuscle
HM01899CD1CthymusMESH:D006548Hernia, Diaphragmatic
HM01899CD1CthymusMESH:D015658HIV Infections
HM01899CD1CthymusMESH:D007674Kidney Diseasesureter
HM01899CD1CthymusMESH:D007674Kidney Diseasespituitary
HM01899CD1CthymusMESH:D007674Kidney Diseaseskidney
HM01899CD1CthymusMESH:D002252Carbon Tetrachloride Poisoning
HM01899CD1CthymusMESH:D001848Bone Diseases, Developmental
HM01899CD1CthymusMESH:D009190Myelodysplastic Syndromes
HM01899CD1CthymusMESH:D009436Neural Tube Defects
HM01899CD1CthymusMESH:D001714Bipolar Disorder
HM01899CD1CthymusMESH:D006402Hematologic Diseasesbone marrow
HM01899CD1CthymusMESH:D015459Leukemia-Lymphoma, Adult T-Cellbone marrow
HM01899CD1CthymusMESH:D020194Unverricht-Lundborg Syndromemuscle
HM01899CD1CthymusMESH:D005234Fatty Liver
HM01899CD1CthymusMESH:D014178Translocation, Genetic
HM01899CD1CthymusMESH:D012559Schizophrenia
HM01899CD1CthymusMESH:D001008Anxiety Disorders
HM01899CD1CthymusMESH:D005317Fetal Growth Retardation
HM01899CD1CthymusMESH:D004831Epilepsies, Myoclonicmuscle
HM01899CD1CthymusMESH:D017563Lung Diseases, Interstitiallung
HM01899CD1CthymusMESH:D014625Vaginal Neoplasmsbone
HM01899CD1CthymusMESH:D014625Vaginal Neoplasms
HM01899CD1CthymusMESH:D017449Dermatitis, Allergic Contactskin
HM01899CD1CthymusMESH:D048629Micronuclei, Chromosome-Defective
HM01899CD1CthymusMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM01899CD1CthymusMESH:D008175Lung Neoplasmslung
HM01899CD1CthymusMESH:D017029Epilepsy, Complex Partialmuscle
HM01899CD1CthymusMESH:D004362Drug Toxicity
HM01899CD1CthymusMESH:D000014Abnormalities, Drug-Induced
HM01899CD1CthymusMESH:D006330Heart Defects, Congenital
HM01899CD1CthymusMESH:D006849Hydrocephalusbrain
HM01899CD1CthymusMESH:D020521Strokeblood vessel
HM01899CD1CthymusMESH:D000550Amblyopiabrain
HM01899CD1CthymusMESH:D000550Amblyopiabrain
HM01899CD1CthymusMESH:D019310Pseudolymphoma
HM01899CD1CthymusMESH:D011471Prostatic Neoplasmsprostate
HM01899CD1CthymusMESH:D013226Status Epilepticusmuscle
HM01899CD1CthymusMESH:D013226Status Epilepticusmuscle
HM01899CD1CthymusMESH:D013226Status Epilepticusmuscle
HM01899CD1CthymusMESH:D007680Kidney Neoplasmskidney
HM01899CD1CthymusMESH:D005315Fetal Diseases