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: C0278110
Disease: Hemiplegia, Crossed
Hemiplegia, Crossed 		5 2 4 0.44 2 0.50
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		10 0 4 0.29 0 0
CUI: C1865322
Disease: MIGRAINE, FAMILIAL HEMIPLEGIC, 2
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 		6 0 3 0.27 0 0
CUI: C0477373
Disease: Other forms of migraine
Other forms of migraine 		2 0 2 0.25 0 0
CUI: C1735856
Disease: Migraine with Typical Aura
Migraine with Typical Aura 		2 0 2 0.25 0 0
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		2 0 2 0.25 0 0
CUI: C1863062
Disease: Episodic quadriplegia
Episodic quadriplegia 		2 0 2 0.25 0 0
CUI: C1865332
Disease: Transient unilateral blurring of vision
Transient unilateral blurring of vision 		2 0 2 0.25 0 0
CUI: C3549447
Disease: ALTERNATING HEMIPLEGIA OF CHILDHOOD 1
ALTERNATING HEMIPLEGIA OF CHILDHOOD 1 		2 0 2 0.25 0 0
CUI: C0270860
Disease: Basilar-Type Migraine
Basilar-Type Migraine 		3 0 2 0.22 0 0
CUI: C0270816
Disease: epilepsy and migraine
epilepsy and migraine 		7 0 2 0.15 0 0
CUI: C0395920
Disease: Migrainous vertigo
Migrainous vertigo 		7 0 2 0.15 0 0
CUI: C0018991
Disease: Hemiplegia
Hemiplegia 		41 6 6 0.14 1 0.11
CUI: C0221163
Disease: Motor Disorders
Motor Disorders 		25 0 4 0.14 0 0
CUI: C0028850
Disease: Ocular Motility Disorders
Ocular Motility Disorders 		9 0 2 0.13 0 0
CUI: C1868681
Disease: DYSTONIA 12
DYSTONIA 12 		9 25 2 0.13 4 0.16
CUI: C1720189
Disease: Episodic Ataxia
Episodic Ataxia 		36 0 5 0.13 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 0.12 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 0.12 0 0
CUI: C0338483
Disease: Migraine with Prolonged Aura
Migraine with Prolonged Aura 		1 0 1 0.12 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 0.12 0 0
CUI: C0581882
Disease: Transient neurological symptoms
Transient neurological symptoms 		1 0 1 0.12 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 0.12 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 0.12 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 0.12 0 0