OPN1MW, opsin 1, medium wave sensitive, 2652

N. diseases: 107; N. variants: 5
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C2931753
Disease: Achromatopsia incomplete, X-linked
Achromatopsia incomplete, X-linked 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2004 2004
CUI: C3887937
Disease: CONE DYSTROPHY 5, X-LINKED
CONE DYSTROPHY 5, X-LINKED 		disease Disease or Syndrome 2 1 0.100 None 0 1
CUI: C0267926
Disease: Postoperative biliary stricture
Postoperative biliary stricture 		disease Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C4551635
Disease: Deuteranopia
Deuteranopia 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C1839612
Disease: MYOPIA 1, X-LINKED
MYOPIA 1, X-LINKED 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C4551767
Disease: Protanopia
Protanopia 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0339530
Disease: Progressive cone-rod dystrophy
Progressive cone-rod dystrophy 		disease Disease or Syndrome 6 0.010 None 1.000 1 2017 2017
CUI: C1719497
Disease: Localized chronic periodontitis
Localized chronic periodontitis 		disease Stomatognathic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2019 2019
CUI: C3159311
Disease: BORNHOLM EYE DISEASE
BORNHOLM EYE DISEASE 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 7 1 0.300 None 1.000 1 2013 2013
CUI: C0155015
Disease: Color Blindness, Red
Color Blindness, Red 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 9 1 0.010 None 1.000 1 2017 2017
CUI: C0701818
Disease: Choledocholithiasis
Choledocholithiasis 		disease Digestive System Diseases Disease or Syndrome 12 0.040 None 0.500 4 2017 2020
CUI: C3826394
Disease: Epilepsy in children
Epilepsy in children 		disease Nervous System Diseases Disease or Syndrome 12 1 0.010 None 1.000 1 2018 2018
CUI: C4275079
Disease: Posterior cortical atrophy syndrome
Posterior cortical atrophy syndrome 		disease Disease or Syndrome 12 8 0.010 None 1.000 1 2011 2011
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 16 9 0.770 strong 1.000 10 2 1995 2019
CUI: C0149520
Disease: Acute Cholecystitis
Acute Cholecystitis 		disease Digestive System Diseases Disease or Syndrome 21 0.010 None 1.000 1 2019 2019
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 24 0.120 None 1.000 2 1989 2017
CUI: C0543968
Disease: Cone dysfunction syndrome
Cone dysfunction syndrome 		disease Disease or Syndrome 25 2 0.010 None 1.000 1 2016 2016
CUI: C1719498
Disease: Generalized chronic periodontitis
Generalized chronic periodontitis 		disease Stomatognathic Diseases Disease or Syndrome 25 4 0.010 None 1.000 1 2019 2019
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus 		disease Eye Diseases; Nervous System Diseases Disease or Syndrome 25 2 0.100 None 0
CUI: C0235272
Disease: Retinal damage
Retinal damage 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Wounds and Injuries Disease or Syndrome 32 1 0.010 None 1.000 1 2019 2019
CUI: C0149778
Disease: Soft Tissue Infection
Soft Tissue Infection 		group Infections Disease or Syndrome 38 0.010 None 1.000 1 2015 2015
CUI: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Sign or Symptom 39 5 0.010 None 1.000 1 2019 2019
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 44 18 0.020 None 1.000 2 1991 1992
CUI: C0751772
Disease: REM Sleep Behavior Disorder
REM Sleep Behavior Disorder 		disease Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 46 16 0.010 None 1.000 1 2019 2019
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		disease Eye Diseases Disease or Syndrome 48 31 0.010 None 1.000 1 2016 2016