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: C0038828
Disease: Superior Mesenteric Artery Syndrome
Superior Mesenteric Artery Syndrome 		2 0 2 0.29 0 0
CUI: C0311262
Disease: Chronic mesenteric ischemia
Chronic mesenteric ischemia 		2 0 2 0.29 0 0
CUI: C0477373
Disease: Other forms of migraine
Other forms of migraine 		2 0 2 0.29 0 0
CUI: C1735856
Disease: Migraine with Typical Aura
Migraine with Typical Aura 		2 0 2 0.29 0 0
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		2 0 2 0.29 0 0
CUI: C1838230
Disease: SPINAL MUSCULAR ATROPHY, TYPE IV
SPINAL MUSCULAR ATROPHY, TYPE IV 		2 0 2 0.29 0 0
CUI: C1865332
Disease: Transient unilateral blurring of vision
Transient unilateral blurring of vision 		2 0 2 0.29 0 0
CUI: C4732793
Disease: Polyminimyoclonus
Polyminimyoclonus 		2 0 2 0.29 0 0
CUI: C0395920
Disease: Migrainous vertigo
Migrainous vertigo 		7 0 3 0.27 0 0
CUI: C0155141
Disease: Acute conjunctivitis
Acute conjunctivitis 		3 0 2 0.25 0 0
CUI: C0270860
Disease: Basilar-Type Migraine
Basilar-Type Migraine 		3 0 2 0.25 0 0
CUI: C0393546
Disease: Oculopharyngeal Spinal Muscular Atrophy
Oculopharyngeal Spinal Muscular Atrophy 		3 0 2 0.25 0 0
CUI: C0549118
Disease: Hemiplegia-hemiconvulsion-epilepsy syndrome
Hemiplegia-hemiconvulsion-epilepsy syndrome 		3 0 2 0.25 0 0
CUI: C0751334
Disease: Progressive Proximal Myelopathic Muscular Atrophy
Progressive Proximal Myelopathic Muscular Atrophy 		3 0 2 0.25 0 0
CUI: C0751335
Disease: Scapuloperoneal Form of Spinal Muscular Atrophy
Scapuloperoneal Form of Spinal Muscular Atrophy 		3 0 2 0.25 0 0
CUI: C1301959
Disease: Bulbar weakness
Bulbar weakness 		3 0 2 0.25 0 0
CUI: C1518715
Disease: Ovarian Fetiform Teratoma
Ovarian Fetiform Teratoma 		3 0 2 0.25 0 0
CUI: C3826237
Disease: Head--Tumors
Head--Tumors 		3 0 2 0.25 0 0
CUI: C4024911
Disease: Acute infantile spinal muscular atrophy
Acute infantile spinal muscular atrophy 		3 0 2 0.25 0 0
CUI: C1864497
Disease: PSORIASIS 2
PSORIASIS 2 		4 0 2 0.22 0 0
CUI: C2931358
Disease: Muscular atrophy, spinal, infantile chronic form
Muscular atrophy, spinal, infantile chronic form 		4 0 2 0.22 0 0
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		10 0 3 0.21 0 0
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
Hemiplegic migraine, familial type 1 		10 0 3 0.21 0 0
CUI: C1854657
Disease: Limb fasciculations
Limb fasciculations 		5 0 2 0.20 0 0
CUI: C2349453
Disease: Familial migraine
Familial migraine 		5 0 2 0.20 0 0