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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM03901NRXN2eyeMESH:D020194Unverricht-Lundborg Syndromemuscle
HM03901NRXN2eyeMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM03901NRXN2eyeMESH:D012135Respiratory Sounds
HM03901NRXN2eyeMESH:D000550Amblyopiabrain
HM03901NRXN2eyeMESH:D000550Amblyopiabrain
HM03901NRXN2eyeMESH:D011014Pneumonialung
HM03901NRXN2eyeMESH:D005911Gliosis
HM03901NRXN2eyeMESH:D008171Lung Diseases
HM03901NRXN2eyeMESH:D008881Migraine Disordersbrain
HM03901NRXN2eyeMESH:D009139Musculoskeletal Abnormalities
HM03901NRXN2eyeMESH:D009436Neural Tube Defects
HM03901NRXN2eyeMESH:D006505Hepatitis
HM03901NRXN2eyeMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM03901NRXN2eyeMESH:D008114Liver Neoplasms, Experimental
HM03901NRXN2eyeMESH:D017563Lung Diseases, Interstitiallung
HM03901NRXN2eyeMESH:D000015Abnormalities, Multiple
HM03901NRXN2eyeMESH:D009190Myelodysplastic Syndromes
HM03901NRXN2eyeMESH:D017029Epilepsy, Complex Partialmuscle
HM03901NRXN2eyeMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM03901NRXN2eyeMESH:D008107Liver Diseasesskin
HM03901NRXN2eyeMESH:D008107Liver Diseasesmuscle
HM03901NRXN2eyeMESH:D008107Liver Diseaseslung
HM03901NRXN2eyeMESH:D008107Liver Diseasesliver
HM03901NRXN2eyeMESH:D019465Craniofacial Abnormalities
HM03901NRXN2eyeMESH:D006932Hyperbilirubinemia
HM03901NRXN2eyeMESH:D004421Dystonia
HM03901NRXN2eyeMESH:D008679Metaplasia
HM03901NRXN2eyeMESH:D005234Fatty Liver
HM03901NRXN2eyeMESH:D008175Lung Neoplasmslung
HM03901NRXN2eyeMESH:D011658Pulmonary Fibrosislung
HM03901NRXN2eyeMESH:D012162Retinal Degenerationeye
HM03901NRXN2eyeMESH:D013226Status Epilepticusmuscle
HM03901NRXN2eyeMESH:D013226Status Epilepticusmuscle
HM03901NRXN2eyeMESH:D013226Status Epilepticusmuscle
HM03901NRXN2eyeMESH:D000382Agricultural Workers' Diseases
HM03901NRXN2eyeMESH:D002100Cachexia
HM03901NRXN2eyeMESH:D006849Hydrocephalusbrain
HM03901NRXN2eyeMESH:D012559Schizophrenia
HM03901NRXN2eyeMESH:D016135Spinal Dysraphismspinal cord
HM03901NRXN2eyeMESH:D019310Pseudolymphoma
HM03901NRXN2eyeMESH:D001848Bone Diseases, Developmental
HM03901NRXN2eyeMESH:D004828Epilepsies, Partialmuscle
HM03901NRXN2eyeMESH:D005315Fetal Diseases
HM03901NRXN2eyeMESH:D004832Epilepsy, Absencemuscle
HM03901NRXN2eyeMESH:D010300Parkinson Diseasenerve
HM03901NRXN2eyeMESH:D009410Nerve Degeneration
HM03901NRXN2eyeMESH:D016535Bronchial Hyperreactivity
HM03901NRXN2eyeMESH:D005355Fibrosis
HM03901NRXN2eyeMESH:D000544Alzheimer Diseasenerve
HM03901NRXN2eyeMESH:D001321Autistic Disorder
HM03901NRXN2eyeMESH:D001714Bipolar Disorder
HM03901NRXN2eyeMESH:D004827Epilepsymuscle
HM03901NRXN2eyeMESH:D010538Peritonitis
HM03901NRXN2eyeMESH:D012640Seizuresmuscle
HM03901NRXN2eyeMESH:D014564Urogenital Abnormalities
HM03901NRXN2eyeMESH:D008103Liver Cirrhosisliver
HM03901NRXN2eyeMESH:D002252Carbon Tetrachloride Poisoning
HM03901NRXN2eyeMESH:D007248Infertility, Male
HM03901NRXN2eyeMESH:D056486Drug-Induced Liver Injury
HM03901NRXN2eyeMESH:D012208Rhabdomyosarcomarectum
HM03901NRXN2eyeMESH:D012208Rhabdomyosarcomaprostate
HM03901NRXN2eyeMESH:D012208Rhabdomyosarcomamuscle
HM03901NRXN2eyeMESH:D000014Abnormalities, Drug-Induced
HM03901NRXN2eyeMESH:D001008Anxiety Disorders
HM03901NRXN2eyeMESH:D001249Asthmalung
HM03901NRXN2eyeMESH:D012128Respiratory Distress Syndrome, Adultlung
HM03901NRXN2eyeMESH:D008106Liver Cirrhosis, Experimental
HM03901NRXN2eyeMESH:D004831Epilepsies, Myoclonicmuscle
HM03901NRXN2eyeMESH:D005317Fetal Growth Retardation
HM03901NRXN2eyeMESH:D001172Arthritis, Rheumatoidbone
HM03901NRXN2eyeMESH:D017114Liver Failure, Acute
HM03901NRXN2eyeMESH:D014178Translocation, Genetic
HM03901NRXN2eyeMESH:D017093Liver Failure