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: C0338483
Disease: Migraine with Prolonged Aura
Migraine with Prolonged Aura 		disease Nervous System Diseases Disease or Syndrome 1 0.020 None 1.000 2 2012 2018
CUI: C0581882
Disease: Transient neurological symptoms
Transient neurological symptoms 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 1 0.010 None 1.000 1 2006 2006
CUI: C1865323
Disease: Migraine, Familial Basilar
Migraine, Familial Basilar 		disease Nervous System Diseases Disease or Syndrome 1 1 0.110 None 1.000 1 1 2005 2005
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		disease Nervous System Diseases Disease or Syndrome 2 4 0.080 None 1.000 8 1 2008 2018
CUI: C3549447
Disease: ALTERNATING HEMIPLEGIA OF CHILDHOOD 1
ALTERNATING HEMIPLEGIA OF CHILDHOOD 1 		disease Disease or Syndrome 2 1 0.610 None 1.000 5 1 2003 2020
CUI: C1735856
Disease: Migraine with Typical Aura
Migraine with Typical Aura 		disease Nervous System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2006 2006
CUI: C0477373
Disease: Other forms of migraine
Other forms of migraine 		group Nervous System Diseases Disease or Syndrome 2 0.200 None 0
CUI: C1863061
Disease: Episodic hemiplegia
Episodic hemiplegia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 2 1 0.100 None 0
CUI: C1863062
Disease: Episodic quadriplegia
Episodic quadriplegia 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.100 None 0
CUI: C1865332
Disease: Transient unilateral blurring of vision
Transient unilateral blurring of vision 		phenotype Finding 2 0.100 None 0
CUI: C0270860
Disease: Basilar-Type Migraine
Basilar-Type Migraine 		disease Nervous System Diseases Disease or Syndrome 3 3 0.030 None 1.000 3 1 2005 2008
CUI: C0521533
Disease: Atrial septal aneurysm
Atrial septal aneurysm 		disease Cardiovascular Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 2018 2018
CUI: C2349453
Disease: Familial migraine
Familial migraine 		disease Disease or Syndrome 5 0.010 None 1.000 1 2015 2015
CUI: C1865322
Disease: MIGRAINE, FAMILIAL HEMIPLEGIC, 2
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 		disease Nervous System Diseases Disease or Syndrome 6 14 0.800 None 1.000 23 13 2003 2020
CUI: C0270816
Disease: epilepsy and migraine
epilepsy and migraine 		disease Disease or Syndrome 7 1 0.310 strong 1.000 2 1 2003 2008
CUI: C0395920
Disease: Migrainous vertigo
Migrainous vertigo 		disease Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 7 1 0.010 None 1.000 1 2006 2006
CUI: C0338488
Disease: Alternating hemiplegia of childhood
Alternating hemiplegia of childhood 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 8 4 0.540 None 1.000 5 2004 2019
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
Hemiplegic migraine, familial type 1 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 10 37 0.200 None 0.917 36 6 2002 2017
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		disease Nervous System Diseases Disease or Syndrome 10 14 0.100 None 1.000 12 1 2004 2019
CUI: C1720416
Disease: Episodic ataxia type 2 (disorder)
Episodic ataxia type 2 (disorder) 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 13 60 0.010 None 1.000 1 2006 2006
CUI: C0220669
Disease: Familial benign neonatal epilepsy
Familial benign neonatal epilepsy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 19 13 0.320 strong 1.000 2 1 2003 2004
CUI: C0238358
Disease: Hypokalemic periodic paralysis
Hypokalemic periodic paralysis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 19 19 0.310 strong 1.000 2 2007 2018
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine 		disease Nervous System Diseases Disease or Syndrome 24 17 0.200 None 1.000 42 9 2002 2019
CUI: C0742038
Disease: Cerebellar signs
Cerebellar signs 		phenotype Sign or Symptom 24 5 0.010 None < 0.001 1 1 2004 2004
CUI: C1557375
Disease: Blurred Vision, CTCAE
Blurred Vision, CTCAE 		phenotype Finding 26 0.100 None 0