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 0.67 0 0
CUI: C0311262
Disease: Chronic mesenteric ischemia
Chronic mesenteric ischemia 		2 0 2 0.67 0 0
CUI: C1838230
Disease: SPINAL MUSCULAR ATROPHY, TYPE IV
SPINAL MUSCULAR ATROPHY, TYPE IV 		2 0 2 0.67 0 0
CUI: C4732793
Disease: Polyminimyoclonus
Polyminimyoclonus 		2 0 2 0.67 0 0
CUI: C0155141
Disease: Acute conjunctivitis
Acute conjunctivitis 		3 0 2 0.50 0 0
CUI: C0393546
Disease: Oculopharyngeal Spinal Muscular Atrophy
Oculopharyngeal Spinal Muscular Atrophy 		3 0 2 0.50 0 0
CUI: C0751334
Disease: Progressive Proximal Myelopathic Muscular Atrophy
Progressive Proximal Myelopathic Muscular Atrophy 		3 0 2 0.50 0 0
CUI: C0751335
Disease: Scapuloperoneal Form of Spinal Muscular Atrophy
Scapuloperoneal Form of Spinal Muscular Atrophy 		3 0 2 0.50 0 0
CUI: C1301959
Disease: Bulbar weakness
Bulbar weakness 		3 0 2 0.50 0 0
CUI: C1518715
Disease: Ovarian Fetiform Teratoma
Ovarian Fetiform Teratoma 		3 0 2 0.50 0 0
CUI: C3826237
Disease: Head--Tumors
Head--Tumors 		3 0 2 0.50 0 0
CUI: C1864497
Disease: PSORIASIS 2
PSORIASIS 2 		4 0 2 0.40 0 0
CUI: C2931358
Disease: Muscular atrophy, spinal, infantile chronic form
Muscular atrophy, spinal, infantile chronic form 		4 0 2 0.40 0 0
CUI: C0270958
Disease: Kocher-Debre-Semelaigne syndrome
Kocher-Debre-Semelaigne syndrome 		1 0 1 0.33 0 0
CUI: C1836437
Disease: B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations
B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations 		1 0 1 0.33 0 0
CUI: C1854657
Disease: Limb fasciculations
Limb fasciculations 		5 0 2 0.33 0 0
CUI: C2750536
Disease: Nemaline Myopathy 3, With Intranuclear Rods
Nemaline Myopathy 3, With Intranuclear Rods 		1 0 1 0.33 0 0
CUI: C2750537
Disease: Myopathy, Actin, Congenital, With Cores
Myopathy, Actin, Congenital, With Cores 		1 0 1 0.33 0 0
CUI: C2931844
Disease: Spinal muscular atrophy 4
Spinal muscular atrophy 4 		1 0 1 0.33 0 0
CUI: C4016747
Disease: SPINAL MUSCULAR ATROPHY, MODIFIER OF
SPINAL MUSCULAR ATROPHY, MODIFIER OF 		1 0 1 0.33 0 0
CUI: C4225181
Disease: MYOPATHY, SCAPULOHUMEROPERONEAL
MYOPATHY, SCAPULOHUMEROPERONEAL 		1 0 1 0.33 0 0
CUI: C0393538
Disease: Muscular Atrophy, Spinal, Type II
Muscular Atrophy, Spinal, Type II 		6 0 2 0.29 0 0
CUI: C0700595
Disease: Spinal Muscular Atrophies of Childhood
Spinal Muscular Atrophies of Childhood 		6 0 2 0.29 0 0
CUI: C4750288
Disease: Spinal muscular atrophy with lower extremity predominance
Spinal muscular atrophy with lower extremity predominance 		6 0 2 0.29 0 0
CUI: C0231666
Disease: Wrist-Drop
Wrist-Drop 		2 0 1 0.25 0 0