GRM2, glutamate metabotropic receptor 2, 2912

N. diseases: 104; N. variants: 1
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: C4529964
Disease: Opioid Abuse and Addiction
Opioid Abuse and Addiction 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2018 2018
CUI: C2945698
Disease: panic symptoms
panic symptoms 		phenotype Sign or Symptom 6 0.010 None 1.000 1 2020 2020
CUI: C0858355
Disease: Addicted to cocaine
Addicted to cocaine 		phenotype Mental or Behavioral Dysfunction 7 2 0.300 None 1.000 1 2013 2013
CUI: C3532942
Disease: Mixed dementia
Mixed dementia 		disease Nervous System Diseases; Mental Disorders; Cardiovascular Diseases Mental or Behavioral Dysfunction 12 2 0.010 None 1.000 1 2011 2011
CUI: C0443306
Disease: Spastic
Spastic 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases Mental or Behavioral Dysfunction 13 0.010 None 1.000 1 1993 1993
CUI: C0746408
Disease: mass lesion
mass lesion 		phenotype Neoplastic Process 15 2 0.010 None 1.000 1 1997 1997
CUI: C0033941
Disease: Psychoses, Substance-Induced
Psychoses, Substance-Induced 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 17 0.300 None 1.000 1 2010 2010
CUI: C0014558
Disease: Uncinate Epilepsy
Uncinate Epilepsy 		disease Nervous System Diseases Disease or Syndrome 23 0.300 None 1.000 1 2008 2008
CUI: C0033937
Disease: Psychoses, Drug
Psychoses, Drug 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 23 1 0.300 None 1.000 1 2010 2010
CUI: C0393672
Disease: Epilepsy, Benign Psychomotor, Childhood
Epilepsy, Benign Psychomotor, Childhood 		disease Nervous System Diseases Disease or Syndrome 23 0.300 None 1.000 1 2008 2008
CUI: C0036939
Disease: Shared Paranoid Disorder
Shared Paranoid Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 27 10 0.010 None 1.000 1 2010 2010
CUI: C0028968
Disease: Olivopontocerebellar Atrophies
Olivopontocerebellar Atrophies 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 28 0.010 None 1.000 1 2002 2002
CUI: C0393682
Disease: Epilepsy, Lateral Temporal
Epilepsy, Lateral Temporal 		disease Nervous System Diseases Disease or Syndrome 29 1 0.300 None 1.000 1 2008 2008
CUI: C0424296
Disease: Social disinhibition
Social disinhibition 		disease Mental Disorders Mental or Behavioral Dysfunction 56 5 0.010 None 1.000 1 2017 2017
CUI: C2063866
Disease: Depressive Disorder, Treatment-Resistant
Depressive Disorder, Treatment-Resistant 		disease Mental Disorders Mental or Behavioral Dysfunction 66 19 0.010 None 1.000 1 2017 2017
CUI: C3496069
Disease: cocaine use
cocaine use 		disease Mental or Behavioral Dysfunction 67 8 0.010 None 1.000 1 2017 2017
CUI: C3887551
Disease: Memory dysfunction
Memory dysfunction 		disease Mental Disorders Mental or Behavioral Dysfunction 70 3 0.010 None 1.000 1 2019 2019
CUI: C0236807
Disease: Amphetamine Abuse
Amphetamine Abuse 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 75 0.300 None 1.000 1 2010 2010
CUI: C0236733
Disease: Amphetamine-Related Disorders
Amphetamine-Related Disorders 		group Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 78 3 0.300 None 1.000 1 2010 2010
CUI: C0236804
Disease: Amphetamine Addiction
Amphetamine Addiction 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 81 2 0.300 None 1.000 1 2010 2010
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 100 110 0.010 None 1.000 1 2017 2017
CUI: C0917796
Disease: Optic Atrophy, Hereditary, Leber
Optic Atrophy, Hereditary, Leber 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases Disease or Syndrome 100 46 0.010 None 1.000 1 2019 2019
CUI: C0034494
Disease: Rabies (disorder)
Rabies (disorder) 		disease Infections Disease or Syndrome 123 0.010 None 1.000 1 2018 2018
CUI: C0087169
Disease: Withdrawal Symptoms
Withdrawal Symptoms 		phenotype Chemically-Induced Disorders; Mental Disorders Sign or Symptom 126 10 0.010 None 1.000 1 2018 2018
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 126 30 0.010 None 1.000 1 2006 2006