Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0424939
Disease: Learning difficulties
Learning difficulties 		6 0 1 0.14 0 0
CUI: C1865322
Disease: MIGRAINE, FAMILIAL HEMIPLEGIC, 2
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 		6 0 1 0.14 0 0
CUI: C0001890
Disease: Akinetic Petit Mal
Akinetic Petit Mal 		7 0 1 0.12 0 0
CUI: C0270816
Disease: epilepsy and migraine
epilepsy and migraine 		7 0 1 0.12 0 0
CUI: C0395920
Disease: Migrainous vertigo
Migrainous vertigo 		7 0 1 0.12 0 0
CUI: C1835265
Disease: Lymphedema, microcephaly and chorioretinopathy syndrome
Lymphedema, microcephaly and chorioretinopathy syndrome 		7 0 1 0.12 0 0
CUI: C4553705
Disease: Absence Seizure Disorder
Absence Seizure Disorder 		7 0 1 0.12 0 0
CUI: C0338488
Disease: Alternating hemiplegia of childhood
Alternating hemiplegia of childhood 		8 0 1 0.11 0 0
CUI: C0476217
Disease: Head movements abnormal
Head movements abnormal 		8 0 1 0.11 0 0
CUI: C0751124
Disease: Epilepsy, Absence, Atypical
Epilepsy, Absence, Atypical 		8 0 1 0.11 0 0
CUI: C4552765
Disease: Epilepsy, Minor
Epilepsy, Minor 		8 0 1 0.11 0 0
CUI: C0028850
Disease: Ocular Motility Disorders
Ocular Motility Disorders 		9 0 1 1.0E-01 0 0
CUI: C0271386
Disease: Vertical Nystagmus
Vertical Nystagmus 		9 0 1 1.0E-01 0 0
CUI: C0393524
Disease: Cerebellar Ataxia, Late Onset
Cerebellar Ataxia, Late Onset 		9 0 1 1.0E-01 0 0
CUI: C0393598
Disease: Idiopathic familial dystonia
Idiopathic familial dystonia 		9 0 1 1.0E-01 0 0
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		10 0 1 9.1E-02 0 0
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
Hemiplegic migraine, familial type 1 		10 0 1 9.1E-02 0 0
CUI: C1853394
Disease: Gaze-evoked horizontal nystagmus
Gaze-evoked horizontal nystagmus 		10 0 1 9.1E-02 0 0
CUI: C4021765
Disease: Morphological abnormality of the central nervous system
Morphological abnormality of the central nervous system 		10 0 1 9.1E-02 0 0
CUI: C2748910
Disease: Rett Syndrome, Atypical
Rett Syndrome, Atypical 		11 0 1 8.3E-02 0 0
CUI: C4551715
Disease: Pigmentary retinopathy
Pigmentary retinopathy 		11 0 1 8.3E-02 0 0
CUI: C4280747
Disease: Choking episodes
Choking episodes 		12 0 1 7.7E-02 0 0
CUI: C0393584
Disease: Benign Hereditary Chorea
Benign Hereditary Chorea 		13 0 1 7.1E-02 0 0
CUI: C0751378
Disease: Neurologic Signs
Neurologic Signs 		13 0 1 7.1E-02 0 0
CUI: C1720416
Disease: Episodic ataxia type 2 (disorder)
Episodic ataxia type 2 (disorder) 		13 0 1 7.1E-02 0 0