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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06078C12orf62parathyroid glandMESH:D004832Epilepsy, Absencemuscle
HM06078C12orf62parathyroid glandMESH:D017563Lung Diseases, Interstitiallung
HM06078C12orf62parathyroid glandMESH:D009190Myelodysplastic Syndromes
HM06078C12orf62parathyroid glandMESH:D019310Pseudolymphoma
HM06078C12orf62parathyroid glandMESH:D008881Migraine Disordersbrain
HM06078C12orf62parathyroid glandMESH:D012208Rhabdomyosarcomarectum
HM06078C12orf62parathyroid glandMESH:D012208Rhabdomyosarcomaprostate
HM06078C12orf62parathyroid glandMESH:D012208Rhabdomyosarcomamuscle
HM06078C12orf62parathyroid glandMESH:D012878Skin Neoplasms
HM06078C12orf62parathyroid glandMESH:D004828Epilepsies, Partialmuscle
HM06078C12orf62parathyroid glandMESH:D004421Dystonia
HM06078C12orf62parathyroid glandMESH:D020194Unverricht-Lundborg Syndromemuscle
HM06078C12orf62parathyroid glandMESH:D056486Drug-Induced Liver Injury
HM06078C12orf62parathyroid glandMESH:D003920Diabetes Mellituspancreas
HM06078C12orf62parathyroid glandMESH:D006973Hypertensionlung
HM06078C12orf62parathyroid glandMESH:D006973Hypertensionheart
HM06078C12orf62parathyroid glandMESH:D006973Hypertensionblood vessel
HM06078C12orf62parathyroid glandMESH:D014564Urogenital Abnormalities
HM06078C12orf62parathyroid glandMESH:D005315Fetal Diseases
HM06078C12orf62parathyroid glandMESH:D000015Abnormalities, Multiple
HM06078C12orf62parathyroid glandMESH:D005234Fatty Liver
HM06078C12orf62parathyroid glandMESH:D008113Liver Neoplasms
HM06078C12orf62parathyroid glandMESH:D008113Liver Neoplasms
HM06078C12orf62parathyroid glandMESH:D008175Lung Neoplasmslung
HM06078C12orf62parathyroid glandMESH:D014178Translocation, Genetic
HM06078C12orf62parathyroid glandMESH:D006330Heart Defects, Congenital
HM06078C12orf62parathyroid glandMESH:D012559Schizophrenia
HM06078C12orf62parathyroid glandMESH:D002294Carcinoma, Squamous Celllung
HM06078C12orf62parathyroid glandMESH:D002294Carcinoma, Squamous Cellliver
HM06078C12orf62parathyroid glandMESH:D002294Carcinoma, Squamous Celllarynx
HM06078C12orf62parathyroid glandMESH:D002294Carcinoma, Squamous Cellkidney
HM06078C12orf62parathyroid glandMESH:D002294Carcinoma, Squamous Celleye
HM06078C12orf62parathyroid glandMESH:D009062Mouth Neoplasms
HM06078C12orf62parathyroid glandMESH:D016135Spinal Dysraphismspinal cord
HM06078C12orf62parathyroid glandMESH:D001749Urinary Bladder Neoplasmsureter
HM06078C12orf62parathyroid glandMESH:D001749Urinary Bladder Neoplasmsbladder
HM06078C12orf62parathyroid glandMESH:D001008Anxiety Disorders
HM06078C12orf62parathyroid glandMESH:D009404Nephrotic Syndromekidney
HM06078C12orf62parathyroid glandMESH:D016393Lymphoma, B-Cell
HM06078C12orf62parathyroid glandMESH:D008664Metal Metabolism, Inborn Errorsskin
HM06078C12orf62parathyroid glandMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM06078C12orf62parathyroid glandMESH:D008664Metal Metabolism, Inborn Errorsliver
HM06078C12orf62parathyroid glandMESH:D008664Metal Metabolism, Inborn Errorskidney
HM06078C12orf62parathyroid glandMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM06078C12orf62parathyroid glandMESH:D011471Prostatic Neoplasmsprostate
HM06078C12orf62parathyroid glandMESH:D011565Psoriasisskin
HM06078C12orf62parathyroid glandMESH:D012640Seizuresmuscle
HM06078C12orf62parathyroid glandMESH:D007333Insulin Resistance
HM06078C12orf62parathyroid glandMESH:D001943Breast Neoplasmsbreast
HM06078C12orf62parathyroid glandMESH:D006457Hemoglobinuria, Paroxysmal
HM06078C12orf62parathyroid glandMESH:D000550Amblyopiabrain
HM06078C12orf62parathyroid glandMESH:D000550Amblyopiabrain
HM06078C12orf62parathyroid glandMESH:D004938Esophageal Neoplasms
HM06078C12orf62parathyroid glandMESH:D014605Uveitiseye
HM06078C12orf62parathyroid glandMESH:D019465Craniofacial Abnormalities
HM06078C12orf62parathyroid glandMESH:D017029Epilepsy, Complex Partialmuscle
HM06078C12orf62parathyroid glandMESH:D019457Chromosome Breakage
HM06078C12orf62parathyroid glandMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM06078C12orf62parathyroid glandMESH:D005355Fibrosis
HM06078C12orf62parathyroid glandMESH:D005885Gingival Hyperplasia
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinoma
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinomauterus
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinoma
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinoma
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinomauterus
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinomathyroid
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinomaskin
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinomaparathyroid gland
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinomaliver
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinomakidney
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinomaeye
HM06078C12orf62parathyroid glandMESH:D000230Adenocarcinomaadrenal gland
HM06078C12orf62parathyroid glandMESH:D013226Status Epilepticusmuscle
HM06078C12orf62parathyroid glandMESH:D013226Status Epilepticusmuscle
HM06078C12orf62parathyroid glandMESH:D013226Status Epilepticusmuscle
HM06078C12orf62parathyroid glandMESH:D009436Neural Tube Defects
HM06078C12orf62parathyroid glandMESH:D004831Epilepsies, Myoclonicmuscle
HM06078C12orf62parathyroid glandMESH:D007674Kidney Diseasesureter
HM06078C12orf62parathyroid glandMESH:D007674Kidney Diseasespituitary
HM06078C12orf62parathyroid glandMESH:D007674Kidney Diseaseskidney
HM06078C12orf62parathyroid glandMESH:D007638Keratoconjunctivitis Siccaeye
HM06078C12orf62parathyroid glandMESH:D009402Nephrosis, Lipoidkidney
HM06078C12orf62parathyroid glandMESH:D005317Fetal Growth Retardation
HM06078C12orf62parathyroid glandMESH:D001321Autistic Disorder
HM06078C12orf62parathyroid glandMESH:D004827Epilepsymuscle
HM06078C12orf62parathyroid glandMESH:D014985Xerophthalmiaeye
HM06078C12orf62parathyroid glandMESH:D001848Bone Diseases, Developmental
HM06078C12orf62parathyroid glandMESH:D013274Stomach Neoplasms
HM06078C12orf62parathyroid glandMESH:D001714Bipolar Disorder
HM06078C12orf62parathyroid glandMESH:D009139Musculoskeletal Abnormalities
HM06078C12orf62parathyroid glandMESH:D000014Abnormalities, Drug-Induced
HM06078C12orf62parathyroid glandMESH:D006849Hydrocephalusbrain