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.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
disease Disease or Syndrome 1 6 0.600 6 6 2013 2017
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
phenotype Finding 1 2 0.400 4 2 2008 2017
Sleep Initiation and Maintenance Disorders
disease Mental Disorders; Nervous System Diseases Disease or Syndrome 4 0.300 1 2002 2002
CUI: C0270541
Disease: Rebound Insomnia
Rebound Insomnia
phenotype Mental Disorders; Nervous System Diseases Sign or Symptom 4 0.300 1 2002 2002
CUI: C0349255
Disease: Nonorganic Insomnia
Nonorganic Insomnia
disease Mental Disorders; Nervous System Diseases Disease or Syndrome 4 0.300 1 2002 2002
CUI: C0393759
Disease: Transient Insomnia
Transient Insomnia
phenotype Mental Disorders; Nervous System Diseases Sign or Symptom 4 0.300 1 2002 2002
CUI: C0751249
Disease: Chronic Insomnia
Chronic Insomnia
disease Mental Disorders; Nervous System Diseases Disease or Syndrome 4 0.300 1 2002 2002
CUI: C0751250
Disease: Psychophysiological Insomnia
Psychophysiological Insomnia
disease Mental Disorders; Nervous System Diseases Disease or Syndrome 4 0.300 1 2002 2002
CUI: C0751251
Disease: Secondary Insomnia
Secondary Insomnia
phenotype Mental Disorders; Nervous System Diseases Sign or Symptom 4 0.300 1 2002 2002
CUI: C0751252
Disease: Sleep Initiation Dysfunction
Sleep Initiation Dysfunction
disease Mental Disorders; Nervous System Diseases Disease or Syndrome 4 0.300 1 2002 2002
CUI: C0270854
Disease: Symptomatic Generalized Epilepsy
Symptomatic Generalized Epilepsy
disease Nervous System Diseases Disease or Syndrome 5 0.010 1.000 1 1993 1993
CUI: C4023479
Disease: EEG with focal sharp slow waves
EEG with focal sharp slow waves
phenotype Finding 5 0.100 0
CUI: C0595948
Disease: Atypical absence seizure
Atypical absence seizure
disease Disease or Syndrome 6 0.100 0
CUI: C1838604
Disease: EPILEPSY, CHILDHOOD ABSENCE, 1
EPILEPSY, CHILDHOOD ABSENCE, 1
disease Disease or Syndrome 6 0.300 0
CUI: C0033139
Disease: Primary Insomnia
Primary Insomnia
disease Mental Disorders; Nervous System Diseases Disease or Syndrome 7 1 0.300 1 2002 2002
CUI: C0541798
Disease: Early Awakening
Early Awakening
phenotype Mental Disorders; Nervous System Diseases Mental or Behavioral Dysfunction 7 1 0.300 1 2002 2002
CUI: C0001890
Disease: Akinetic Petit Mal
Akinetic Petit Mal
disease Nervous System Diseases Disease or Syndrome 8 0.300 1 2008 2008
CUI: C0751124
Disease: Epilepsy, Absence, Atypical
Epilepsy, Absence, Atypical
disease Nervous System Diseases Disease or Syndrome 8 0.300 1 2008 2008
CUI: C4317339
Disease: Juvenile Absence Epilepsy
Juvenile Absence Epilepsy
disease Nervous System Diseases Disease or Syndrome 8 0.300 1 2008 2008
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 9 0.320 1.000 2 2015 2016
CUI: C1850601
Disease: Abnormality of brainstem morphology
Abnormality of brainstem morphology
phenotype Finding 10 0.100 0
CUI: C4281785
Disease: Childhood Absence Epilepsy
Childhood Absence Epilepsy
disease Nervous System Diseases Disease or Syndrome 11 0.300 1 2008 2008
CUI: C1836508
Disease: Generalized tonic seizures
Generalized tonic seizures
phenotype Finding 11 1 0.100 0
CUI: C0085639
Disease: Falls
Falls
phenotype Finding 13 0.100 0
CUI: C1836509
Disease: Hypotonic seizures
Hypotonic seizures
phenotype Finding 15 0.100 0