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 0.50 0 0
CUI: C0311262
Disease: Chronic mesenteric ischemia
Chronic mesenteric ischemia 		2 0 2 0.50 0 0
CUI: C1838230
Disease: SPINAL MUSCULAR ATROPHY, TYPE IV
SPINAL MUSCULAR ATROPHY, TYPE IV 		2 0 2 0.50 0 0
CUI: C4732793
Disease: Polyminimyoclonus
Polyminimyoclonus 		2 0 2 0.50 0 0
CUI: C0155141
Disease: Acute conjunctivitis
Acute conjunctivitis 		3 0 2 0.40 0 0
CUI: C0393546
Disease: Oculopharyngeal Spinal Muscular Atrophy
Oculopharyngeal Spinal Muscular Atrophy 		3 0 2 0.40 0 0
CUI: C0751334
Disease: Progressive Proximal Myelopathic Muscular Atrophy
Progressive Proximal Myelopathic Muscular Atrophy 		3 0 2 0.40 0 0
CUI: C0751335
Disease: Scapuloperoneal Form of Spinal Muscular Atrophy
Scapuloperoneal Form of Spinal Muscular Atrophy 		3 0 2 0.40 0 0
CUI: C1301959
Disease: Bulbar weakness
Bulbar weakness 		3 0 2 0.40 0 0
CUI: C1518715
Disease: Ovarian Fetiform Teratoma
Ovarian Fetiform Teratoma 		3 0 2 0.40 0 0
CUI: C3826237
Disease: Head--Tumors
Head--Tumors 		3 0 2 0.40 0 0
CUI: C4024911
Disease: Acute infantile spinal muscular atrophy
Acute infantile spinal muscular atrophy 		3 0 2 0.40 0 0
CUI: C2931358
Disease: Muscular atrophy, spinal, infantile chronic form
Muscular atrophy, spinal, infantile chronic form 		4 0 2 0.33 0 0
CUI: C1854657
Disease: Limb fasciculations
Limb fasciculations 		5 0 2 0.29 0 0
CUI: C0270958
Disease: Kocher-Debre-Semelaigne syndrome
Kocher-Debre-Semelaigne syndrome 		1 0 1 0.25 0 0
CUI: C0393538
Disease: Muscular Atrophy, Spinal, Type II
Muscular Atrophy, Spinal, Type II 		6 0 2 0.25 0 0
CUI: C0700595
Disease: Spinal Muscular Atrophies of Childhood
Spinal Muscular Atrophies of Childhood 		6 0 2 0.25 0 0
CUI: C1290049
Disease: Plaque morphea
Plaque morphea 		1 0 1 0.25 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 0.25 0 0
CUI: C2930842
Disease: Familial pityriasis rubra pilaris
Familial pityriasis rubra pilaris 		1 0 1 0.25 0 0
CUI: C2931844
Disease: Spinal muscular atrophy 4
Spinal muscular atrophy 4 		1 0 1 0.25 0 0
CUI: C4016747
Disease: SPINAL MUSCULAR ATROPHY, MODIFIER OF
SPINAL MUSCULAR ATROPHY, MODIFIER OF 		1 0 1 0.25 0 0
CUI: C4017074
Disease: PSORIASIS 2, PUSTULAR
PSORIASIS 2, PUSTULAR 		1 1 1 0.25 1 7.1E-02
CUI: C4055160
Disease: Deep Circumscribed Morphea
Deep Circumscribed Morphea 		1 0 1 0.25 0 0
CUI: C4750288
Disease: Spinal muscular atrophy with lower extremity predominance
Spinal muscular atrophy with lower extremity predominance 		6 0 2 0.25 0 0