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.
Epilepsy, Nocturnal Frontal Lobe, Type 1
disease Nervous System Diseases Disease or Syndrome 1 2 0.700 None 1.000 4 2 1995 2003
CUI: C4049182
Disease: Idiopathic partial epilepsy
Idiopathic partial epilepsy
disease Disease or Syndrome 2 0.020 None 1.000 2 1997 2003
Epilepsy, Nocturnal Frontal Lobe, Type 3
disease Nervous System Diseases Disease or Syndrome 2 4 0.100 None 0 1
CUI: C0265482
Disease: Ring Chromosome 20 Syndrome
Ring Chromosome 20 Syndrome
disease Pathological Conditions, Signs and Symptoms Congenital Abnormality 3 0.010 None 1.000 1 2008 2008
Epilepsy, Nocturnal Frontal Lobe, Type 4
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3 11 0.100 None 0 2
CUI: C0393671
Disease: Frontal Epilepsy, Benign, Childhood
Frontal Epilepsy, Benign, Childhood
disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 3 2003 2007
CUI: C0393683
Disease: Epilepsy, Supplementary Motor
Epilepsy, Supplementary Motor
disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 3 2003 2007
CUI: C0393684
Disease: Epilepsy, Cingulate
Epilepsy, Cingulate
disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 3 2003 2007
CUI: C0393688
Disease: Epilepsy, Opercular
Epilepsy, Opercular
disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 3 2003 2007
CUI: C0751642
Disease: Epilepsy, Anterior Fronto-Polar
Epilepsy, Anterior Fronto-Polar
disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 3 2003 2007
CUI: C0751643
Disease: Epilepsy, Orbito-Frontal
Epilepsy, Orbito-Frontal
disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 3 2003 2007
CUI: C0393719
Disease: Nocturnal epilepsy
Nocturnal epilepsy
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 4 2 0.010 None 1.000 1 2009 2009
CUI: C0004310
Disease: Auditory Perceptual Disorders
Auditory Perceptual Disorders
group Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 5 0.010 None 1.000 1 2019 2019
CUI: C4543822
Disease: Gaming disorder
Gaming disorder
disease Mental Disorders Mental or Behavioral Dysfunction 6 2 0.010 None 1.000 1 1 2017 2017
CUI: C0751508
Disease: Long Sleeper Syndrome
Long Sleeper Syndrome
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Disease or Syndrome 7 0.300 None 1.000 1 2005 2005
CUI: C0751510
Disease: Sleep-Related Neurogenic Tachypnea
Sleep-Related Neurogenic Tachypnea
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Disease or Syndrome 7 0.300 None 1.000 1 2005 2005
CUI: C0751511
Disease: Subwakefullness Syndrome
Subwakefullness Syndrome
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Disease or Syndrome 7 0.300 None 1.000 1 2005 2005
CUI: C0751509
Disease: Short Sleeper Syndrome
Short Sleeper Syndrome
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Disease or Syndrome 8 1 0.300 None 1.000 1 2005 2005
Epilepsy, Partial, with Variable Foci
disease Nervous System Diseases Disease or Syndrome 8 24 0.010 None 1.000 1 2018 2018
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 9 20 0.010 None 1.000 1 2009 2009
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion
disease Nervous System Diseases Disease or Syndrome 9 7 0.010 None 1.000 1 2009 2009
CUI: C0085541
Disease: Epilepsy, Frontal Lobe
Epilepsy, Frontal Lobe
disease Nervous System Diseases Disease or Syndrome 10 0.400 None 1.000 14 1998 2014
CUI: C0271583
Disease: ACTH Deficiency, Isolated
ACTH Deficiency, Isolated
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 11 11 0.100 None 0 1
TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)
phenotype Finding 12 0.500 limited 1.000 1 2003 2003
CUI: C4042891
Disease: Sleep Wake Disorders
Sleep Wake Disorders
group Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 12 0.300 None 1.000 1 2005 2005