* We recommend a score >= 0.08 for meaningful Gene-Disease associations

GeneID Gene_Symbol DisGeNet_diseaseID Disease_name DisGeNet score DisGeNet_sourceDB
6010RHOC0035334Retinitis Pigmentosa0.708339779041496BEFREE;CTD_human;GAD;HPO;LHGDN;ORPHANET
6010RHOC0339535Night blindness, congenital stationary0.60357144819477BEFREE;CTD_human;HPO;ORPHANET
6010RHOC1864869Night Blindness, Congenital Stationary, Autosomal Dominant 10.48CTD_human;MGD;UNIPROT
6010RHOC3151001Retinitis Pigmentosa 40.48CTD_human;MGD;UNIPROT
6010RHOC0311338Fundus Albipunctatus0.400549453568426BEFREE;CTD_human;ORPHANET
6010RHOC0028077Night Blindness0.20678830169338BEFREE;GAD;HPO;LHGDN
6010RHOC1405854Retinitis punctata albescens (disorder)0.202956482091714BEFREE;GAD;ORPHANET
6010RHOC1306122Oguchi disease0.202472541057918BEFREE;HPO
6010RHOC0085636Photophobia0.200824180352639BEFREE;HPO
6010RHOC3551052Night blindness, stationary0.200549453568426BEFREE;HPO
6010RHOC0025362Mental Retardation0.200274726784213BEFREE;HPO
6010RHOC3714756Intellectual Disability0.200274726784213BEFREE;HPO
6010RHOC0017601Glaucoma0.2HPO
6010RHOC0018777Conductive hearing loss0.2HPO
6010RHOC0018784Sensorineural Hearing Loss (disorder)0.2HPO
6010RHOC0020459Hyperinsulinism0.2HPO
6010RHOC0020619Hypogonadism0.2HPO
6010RHOC0022578Keratoconus0.2HPO
6010RHOC0028738Nystagmus0.2HPO
6010RHOC0028754Obesity0.2HPO
6010RHOC0029089Ophthalmoplegia0.2HPO
6010RHOC0029124Optic Atrophy0.2HPO
6010RHOC0035304Retinal Degeneration0.2CTD_human
6010RHOC0086543Cataract0.2HPO
6010RHOC0234632Reduced visual acuity0.2HPO
6010RHOC0266423Congenital anomaly of testis0.2HPO
6010RHOC0266435Congenital hypoplasia of penis0.2HPO
6010RHOC0271183Severe myopia0.2HPO
6010RHOC0271215Blindness, Legal0.2HPO
6010RHOC0423414Retinal flecking0.2HPO
6010RHOC0423903Low intelligence0.2HPO
6010RHOC0456909Blind Vision0.2HPO
6010RHOC0476397Electroretinogram abnormal0.2HPO
6010RHOC0917816Mental deficiency0.2HPO
6010RHOC1298695Hypoplasia of optic disc0.2HPO
6010RHOC1510497Lens Opacities0.2HPO
6010RHOC1720508Retinal pigment epithelial abnormality0.2HPO
6010RHOC1836926Fundus with peripheral 'bony spicules'0.2HPO
6010RHOC1837087Macular pigmentary changes0.2HPO
6010RHOC1839025Decreased amplitudes on flash visual electroretinogram0.2HPO
6010RHOC1839764Broad flat nasal bridge0.2HPO
6010RHOC1840077Anteverted nostril0.2HPO
6010RHOC1843367Poor school performance0.2HPO
6010RHOC1849367Nasal bridge wide0.2HPO
6010RHOC1862475Abnormality of retinal pigmentation0.2HPO
6010RHOC3887875Visual field defects0.2HPO
6010RHOC4020876Dull intelligence0.2HPO
6010RHOC4020885Difficulties with night vision0.2HPO
6010RHOC4020887Photodysphoria0.2HPO
6010RHOC4020899Autosomal recessive predisposition0.2HPO
6010RHOC4021786Atypical scarring of skin0.2HPO
6010RHOC4024753Abnormality of the retinal vasculature0.2HPO
6010RHOC4024756Abnormality of macular pigmentation0.2HPO
6010RHOC4024818Night blindness, progressive0.2HPO
6010RHOC4048798Night blindness, congenital stationary, complete0.2HPO
6010RHOC0339525Autosomal dominant retinitis pigmentosa0.0257588051814015BEFREE;GAD
6010RHOC0035309Retinal Diseases0.0102942373535208BEFREE;GAD;LHGDN
6010RHOC0027627Neoplasm Metastasis0.0019230874894917BEFREE
6010RHOC1998028Photoreceptor degeneration0.0019230874894917BEFREE
6010RHOC0339526Autosomal recessive retinitis pigmentosa0.0013736339210655BEFREE
6010RHOC3887505DYSFUNCTION - SKIN DISORDERS0.0013736339210655BEFREE
6010RHOC1285162Degenerative disorder0.0010989071368524BEFREE
6010RHOC0011884Diabetic Retinopathy0.0008241803526393BEFREE
6010RHOC0524851Neurodegenerative Disorders0.0008241803526393BEFREE
6010RHOC0003873Rheumatoid Arthritis0.0005494535684262BEFREE
6010RHOC0010674Cystic Fibrosis0.0005494535684262BEFREE
6010RHOC0025202melanoma0.0005494535684262BEFREE
6010RHOC0596263Carcinogenesis0.0005494535684262BEFREE
6010RHOC0854723Retinal Dystrophies0.0005494535684262BEFREE
6010RHOC1272174Scotopic sensitivity0.0005494535684262BEFREE
6010RHOC0006118Brain Neoplasms0.0002747267842131BEFREE
6010RHOC0007131Non-Small Cell Lung Carcinoma0.0002747267842131BEFREE
6010RHOC0007134Renal Cell Carcinoma0.0002747267842131BEFREE
6010RHOC0008525Choroideremia0.0002747267842131BEFREE
6010RHOC0024437Macular degeneration0.0002747267842131BEFREE
6010RHOC0027819Neuroblastoma0.0002747267842131BEFREE
6010RHOC0031941Pineal Gland Neoplasm0.0002747267842131BEFREE
6010RHOC0034951Refractive Errors0.0002747267842131BEFREE
6010RHOC0035220Respiratory Distress Syndrome, Newborn0.0002747267842131BEFREE
6010RHOC0035333Retinitis0.0002747267842131BEFREE
6010RHOC0035335Retinoblastoma0.0002747267842131BEFREE
6010RHOC0036631Seminoma0.0002747267842131BEFREE
6010RHOC0038454Cerebrovascular accident0.0002747267842131BEFREE
6010RHOC0205851Germ cell tumor0.0002747267842131BEFREE
6010RHOC0206139Lichen Planus, Oral0.0002747267842131BEFREE
6010RHOC0220620Gastrointestinal Carcinoid Tumor0.0002747267842131BEFREE
6010RHOC0220701RETINITIS PIGMENTOSA 10.0002747267842131BEFREE
6010RHOC0233794Memory impairment0.0002747267842131BEFREE
6010RHOC0242383Age related macular degeneration0.0002747267842131BEFREE
6010RHOC0278601Inflammatory Breast Carcinoma0.0002747267842131BEFREE
6010RHOC0279000Liver and Intrahepatic Biliary Tract Carcinoma0.0002747267842131BEFREE
6010RHOC0334070Maturation defect0.0002747267842131BEFREE
6010RHOC0339510Vitelliform Macular Dystrophy0.0002747267842131BEFREE
6010RHOC0345904Malignant neoplasm of liver0.0002747267842131BEFREE
6010RHOC0376358Malignant neoplasm of prostate0.0002747267842131BEFREE
6010RHOC0600139Prostate carcinoma0.0002747267842131BEFREE
6010RHOC0700095Central neuroblastoma0.0002747267842131BEFREE
6010RHOC1411966Clostridium; difficile (disorder)0.0002747267842131BEFREE
6010RHOC1458155Mammary Neoplasms0.0002747267842131BEFREE
6010RHOC1842475Retinitis Pigmentosa 70.0002747267842131BEFREE
6010RHOC1961099Precursor T-Cell Lymphoblastic Leukemia-Lymphoma0.0002747267842131BEFREE
6010RHOC2239176Liver carcinoma0.0002747267842131BEFREE
6010RHOC3825718Retina--Diseases0.0002747267842131BEFREE