CNTF, ciliary neurotrophic factor, 1270

N. diseases: 114; N. variants: 3
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: C0748375
Disease: retinal neuropathy
retinal neuropathy 		disease Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0848257
Disease: Schizophrenic psychoses
Schizophrenic psychoses 		disease Mental or Behavioral Dysfunction 2 0.020 None 1.000 2 1996 1998
CUI: C0339480
Disease: Parafoveal telangiectasia
Parafoveal telangiectasia 		disease Disease or Syndrome 4 0.010 None 1.000 1 2016 2016
CUI: C1839942
Disease: Retinal fibrosis
Retinal fibrosis 		disease Acquired Abnormality 4 0.010 None 1.000 1 2016 2016
CUI: C1848947
Disease: COLD-INDUCED SWEATING SYNDROME 1
COLD-INDUCED SWEATING SYNDROME 1 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 4 20 0.010 None 1.000 1 2017 2017
CUI: C4521693
Disease: Telangiectasia of macula lutea
Telangiectasia of macula lutea 		disease Disease or Syndrome 4 0.010 None 1.000 1 2016 2016
CUI: C1963788
Disease: Peripheral nerve lesion
Peripheral nerve lesion 		disease Nervous System Diseases Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C3888461
Disease: Dry age-related macular degeneration
Dry age-related macular degeneration 		phenotype Anatomical Abnormality 11 1 0.010 None 1.000 1 2013 2013
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		disease Disease or Syndrome 15 3 0.010 None 1.000 1 1997 1997
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 20 14 0.020 None 1.000 2 2013 2015
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 26 63 0.020 None 1.000 2 2013 2015
CUI: C1837475
Disease: Insulin-Like Growth Factor I Deficiency
Insulin-Like Growth Factor I Deficiency 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 28 3 0.010 None 1.000 1 2019 2019
CUI: C0004606
Disease: Nonproliferative diabetic retinopathy
Nonproliferative diabetic retinopathy 		disease Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 41 1 0.010 None 1.000 1 2017 2017
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 42 24 0.010 None 1.000 1 2009 2009
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Sign or Symptom 77 3 0.010 None 1.000 1 2000 2000
CUI: C0393819
Disease: Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 82 4 0.010 None 1.000 1 2002 2002
CUI: C0595936
Disease: Aqueous Humor Disorders
Aqueous Humor Disorders 		disease Eye Diseases Disease or Syndrome 85 1 0.010 None 1.000 1 2017 2017
CUI: C0036646
Disease: Age-related cataract
Age-related cataract 		disease Eye Diseases Acquired Abnormality 92 15 0.010 None 1.000 1 2017 2017
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies 		disease Nervous System Diseases Disease or Syndrome 104 4 0.010 None 1.000 1 2009 2009
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 122 78 0.300 None 1.000 1 2001 2001
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration 		phenotype Eye Diseases Pathologic Function 125 2 0.010 None 1.000 1 2003 2003
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 126 61 0.010 None 1.000 1 1998 1998
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
Amyotrophic Lateral Sclerosis, Familial 		disease Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 130 68 0.320 None 1.000 2 1995 2002
CUI: C0013473
Disease: Eating Disorders
Eating Disorders 		group Mental Disorders Mental or Behavioral Dysfunction 133 42 0.010 None 1.000 1 2010 2010
CUI: C1998028
Disease: Photoreceptor degeneration
Photoreceptor degeneration 		disease Eye Diseases Disease or Syndrome 136 16 0.040 None 1.000 4 2003 2018