PDYN, prodynorphin, 5173

N. diseases: 197; N. variants: 13
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: C0036659
Disease: Sensation Disorders
Sensation Disorders 		group Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 1 0.300 None 1.000 1 2009 2009
CUI: C0270712
Disease: Late cortical cerebellar atrophy
Late cortical cerebellar atrophy 		disease Nervous System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2009 2009
CUI: C0751497
Disease: Special Senses Disorders
Special Senses Disorders 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 1 0.300 None 1.000 1 2009 2009
CUI: C1853250
Disease: SPINOCEREBELLAR ATAXIA 23
SPINOCEREBELLAR ATAXIA 23 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 2 7 0.740 None 1.000 5 7 2010 2013
CUI: C0393520
Disease: Harding ataxia
Harding ataxia 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.010 None 1.000 1 1998 1998
CUI: C4237239
Disease: Opioid use disorder, severe
Opioid use disorder, severe 		disease Mental or Behavioral Dysfunction 2 0.010 None 1.000 1 2019 2019
CUI: C4310780
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23 		disease Disease or Syndrome 2 2 0.010 None 1.000 1 2019 2019
CUI: C4518339
Disease: Sporadic adult-onset ataxia of unknown etiology
Sporadic adult-onset ataxia of unknown etiology 		phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Sign or Symptom 3 0.020 None 1.000 2 1995 1998
CUI: C3807295
Disease: CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT
CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT 		disease Disease or Syndrome 3 3 0.010 None 1.000 1 2017 2017
CUI: C0030200
Disease: Pain, Intractable
Pain, Intractable 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 6 0.010 None 1.000 1 2012 2012
CUI: C0152027
Disease: Sensory Disorders
Sensory Disorders 		group Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 6 0.300 None 1.000 1 2009 2009
CUI: C0232766
Disease: Asterixis
Asterixis 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 7 0.300 None 1.000 1 2011 2011
CUI: C0454606
Disease: Oral Dyskinesia
Oral Dyskinesia 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 7 0.300 None 1.000 1 2011 2011
CUI: C0752196
Disease: Ballismus
Ballismus 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 7 0.300 None 1.000 1 2011 2011
CUI: C0221169
Disease: Hemiballismus
Hemiballismus 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 9 0.300 None 1.000 1 2011 2011
CUI: C1853767
Disease: Impaired distal vibration sensation
Impaired distal vibration sensation 		phenotype Finding 10 1 0.100 None 0
CUI: C0020440
Disease: Hypercapnia
Hypercapnia 		phenotype Pathological Conditions, Signs and Symptoms Finding 11 0.300 None 1.000 1 2001 2001
CUI: C4551628
Disease: Opiate Abuse
Opiate Abuse 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 12 0.010 None 1.000 1 2013 2013
CUI: C1861736
Disease: SPINOCEREBELLAR ATAXIA 31 (disorder)
SPINOCEREBELLAR ATAXIA 31 (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 13 0.010 None 1.000 1 2012 2012
CUI: C0037952
Disease: Spinocerebellar Degeneration
Spinocerebellar Degeneration 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 14 1 0.010 None 1.000 1 1998 1998
CUI: C0751088
Disease: Dyskinesia, Medication-Induced
Dyskinesia, Medication-Induced 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders Disease or Syndrome 15 0.300 None 1.000 2 1998 2011
CUI: C1856691
Disease: Impaired proprioception
Impaired proprioception 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 15 3 0.100 None 0
CUI: C0233750
Disease: Hysterical amnesia
Hysterical amnesia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 17 0.300 None 1.000 1 1995 1995
CUI: C0233796
Disease: Temporary Amnesia
Temporary Amnesia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 17 0.300 None 1.000 1 1995 1995
CUI: C0236795
Disease: Dissociative Amnesia
Dissociative Amnesia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 17 0.300 None 1.000 1 1995 1995