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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01782PLXDC1thymusMESH:D001321Autistic Disorder
HM01782PLXDC1thymusMESH:D013226Status Epilepticusmuscle
HM01782PLXDC1thymusMESH:D013226Status Epilepticusmuscle
HM01782PLXDC1thymusMESH:D013226Status Epilepticusmuscle
HM01782PLXDC1thymusMESH:D006932Hyperbilirubinemia
HM01782PLXDC1thymusMESH:D020194Unverricht-Lundborg Syndromemuscle
HM01782PLXDC1thymusMESH:D008106Liver Cirrhosis, Experimental
HM01782PLXDC1thymusMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM01782PLXDC1thymusMESH:D008103Liver Cirrhosisliver
HM01782PLXDC1thymusMESH:D001008Anxiety Disorders
HM01782PLXDC1thymusMESH:D004832Epilepsy, Absencemuscle
HM01782PLXDC1thymusMESH:D000014Abnormalities, Drug-Induced
HM01782PLXDC1thymusMESH:D005355Fibrosis
HM01782PLXDC1thymusMESH:D017563Lung Diseases, Interstitiallung
HM01782PLXDC1thymusMESH:D004828Epilepsies, Partialmuscle
HM01782PLXDC1thymusMESH:D004827Epilepsymuscle
HM01782PLXDC1thymusMESH:D000550Amblyopiabrain
HM01782PLXDC1thymusMESH:D000550Amblyopiabrain
HM01782PLXDC1thymusMESH:D012208Rhabdomyosarcomarectum
HM01782PLXDC1thymusMESH:D012208Rhabdomyosarcomaprostate
HM01782PLXDC1thymusMESH:D012208Rhabdomyosarcomamuscle
HM01782PLXDC1thymusMESH:D000015Abnormalities, Multiple
HM01782PLXDC1thymusMESH:D012640Seizuresmuscle
HM01782PLXDC1thymusMESH:D056486Drug-Induced Liver Injury
HM01782PLXDC1thymusMESH:D006849Hydrocephalusbrain
HM01782PLXDC1thymusMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM01782PLXDC1thymusMESH:D001848Bone Diseases, Developmental
HM01782PLXDC1thymusMESH:D005315Fetal Diseases
HM01782PLXDC1thymusMESH:D008114Liver Neoplasms, Experimental
HM01782PLXDC1thymusMESH:D017093Liver Failure
HM01782PLXDC1thymusMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM01782PLXDC1thymusMESH:D017029Epilepsy, Complex Partialmuscle
HM01782PLXDC1thymusMESH:D005317Fetal Growth Retardation
HM01782PLXDC1thymusMESH:D004831Epilepsies, Myoclonicmuscle
HM01782PLXDC1thymusMESH:D004421Dystonia
HM01782PLXDC1thymusMESH:D014564Urogenital Abnormalities
HM01782PLXDC1thymusMESH:D002252Carbon Tetrachloride Poisoning
HM01782PLXDC1thymusMESH:D006505Hepatitis
HM01782PLXDC1thymusMESH:D009190Myelodysplastic Syndromes
HM01782PLXDC1thymusMESH:D009436Neural Tube Defects
HM01782PLXDC1thymusMESH:D008107Liver Diseasesskin
HM01782PLXDC1thymusMESH:D008107Liver Diseasesmuscle
HM01782PLXDC1thymusMESH:D008107Liver Diseaseslung
HM01782PLXDC1thymusMESH:D008107Liver Diseasesliver
HM01782PLXDC1thymusMESH:D014178Translocation, Genetic
HM01782PLXDC1thymusMESH:D005234Fatty Liver
HM01782PLXDC1thymusMESH:D017114Liver Failure, Acute
HM01782PLXDC1thymusMESH:D016135Spinal Dysraphismspinal cord
HM01782PLXDC1thymusMESH:D012559Schizophrenia
HM01782PLXDC1thymusMESH:D019310Pseudolymphoma
HM01782PLXDC1thymusMESH:D001714Bipolar Disorder
HM01782PLXDC1thymusMESH:D019465Craniofacial Abnormalities
HM01782PLXDC1thymusMESH:D008881Migraine Disordersbrain
HM01782PLXDC1thymusMESH:D009139Musculoskeletal Abnormalities