PRKCG, protein kinase C gamma, 5582

N. diseases: 63; N. variants: 30
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: C1854369
Disease: Spinocerebellar ataxia 14
Spinocerebellar ataxia 14
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 1 25 0.710 1.000 25 25 1993 2015
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
group Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms Mental or Behavioral Dysfunction 2502 53 0.500 limited 2 2004 2012
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 115 3 0.400 1.000 28 1 2004 2015
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
phenotype Nervous System Diseases; Pathological Conditions, Signs and Symptoms Sign or Symptom 118 3 0.300 2 2010 2016
CUI: C0458247
Disease: Allodynia
Allodynia
phenotype Nervous System Diseases; Pathological Conditions, Signs and Symptoms Finding 83 0.300 2 2010 2016
CUI: C0751214
Disease: Hyperalgesia, Thermal
Hyperalgesia, Thermal
phenotype Nervous System Diseases; Pathological Conditions, Signs and Symptoms Sign or Symptom 108 0.300 2 2010 2016
CUI: C0751213
Disease: Tactile Allodynia
Tactile Allodynia
phenotype Nervous System Diseases; Pathological Conditions, Signs and Symptoms Sign or Symptom 88 0.300 2 2010 2016
CUI: C2936719
Disease: Mechanical Allodynia
Mechanical Allodynia
phenotype Nervous System Diseases; Pathological Conditions, Signs and Symptoms Sign or Symptom 107 3 0.300 2 2010 2016
CUI: C0751212
Disease: Hyperalgesia, Secondary
Hyperalgesia, Secondary
phenotype Nervous System Diseases; Pathological Conditions, Signs and Symptoms Sign or Symptom 83 0.300 2 2010 2016
CUI: C0751211
Disease: Hyperalgesia, Primary
Hyperalgesia, Primary
phenotype Nervous System Diseases; Pathological Conditions, Signs and Symptoms Sign or Symptom 84 0.300 2 2010 2016
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 54 0.300 1 2010 2010
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 78 3 0.300 1 2010 2010
CUI: C0040997
Disease: Trigeminal Neuralgia
Trigeminal Neuralgia
disease Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 32 0.300 1 2016 2016
CUI: C0393787
Disease: Secondary Trigeminal Neuralgia
Secondary Trigeminal Neuralgia
disease Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 12 0.300 1 2016 2016
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
disease Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms Mental or Behavioral Dysfunction 1031 0.300 1 2012 2012
CUI: C0393786
Disease: Trigeminal Neuralgia, Idiopathic
Trigeminal Neuralgia, Idiopathic
disease Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 12 0.300 1 2016 2016
CUI: C0752122
Disease: Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 4
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 36 0.300 1 2010 2010
CUI: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 45 4 0.300 1 2010 2010
Spinocerebellar Ataxia Type 6 (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 47 8 0.300 1 2010 2010
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 71 1 0.300 1 2010 2010
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial
disease Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms Mental or Behavioral Dysfunction 137 0.300 1 2012 2012
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
disease Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms Mental or Behavioral Dysfunction 195 2 0.300 1 2012 2012
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 297 104 0.300 limited 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 166 0.300 strong 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia
phenotype Nervous System Diseases; Pathological Conditions, Signs and Symptoms Sign or Symptom 82 5 0.110 1.000 1 2007 2007