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: C0154681
Disease: Anterior Horn Cell Disease
Anterior Horn Cell Disease 		8 0 4 0.21 0 0
CUI: C1865384
Disease: Amyotrophy, monomelic
Amyotrophy, monomelic 		15 0 5 0.20 0 0
CUI: C4016314
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO 		3 0 3 0.20 0 0
CUI: C0033790
Disease: Pseudobulbar Palsy
Pseudobulbar Palsy 		13 0 4 0.17 0 0
CUI: C0700595
Disease: Spinal Muscular Atrophies of Childhood
Spinal Muscular Atrophies of Childhood 		6 0 3 0.17 0 0
CUI: C0393547
Disease: Bulbospinal Neuronopathy
Bulbospinal Neuronopathy 		7 0 3 0.16 0 0
CUI: C4020690
Disease: Abnormality of peripheral nerve conduction
Abnormality of peripheral nerve conduction 		8 0 3 0.15 0 0
CUI: C0393541
Disease: Distal Spinal Muscular Atrophy
Distal Spinal Muscular Atrophy 		16 0 4 0.15 0 0
CUI: C0270763
Disease: Familial Motor Neuron Disease
Familial Motor Neuron Disease 		9 0 3 0.14 0 0
CUI: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy 		9 0 3 0.14 0 0
CUI: C1858517
Disease: SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1
SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1 		10 0 3 0.14 0 0
CUI: C4024957
Disease: Proximal spinal muscular atrophy
Proximal spinal muscular atrophy 		10 0 3 0.14 0 0
CUI: C0038828
Disease: Superior Mesenteric Artery Syndrome
Superior Mesenteric Artery Syndrome 		2 0 2 0.13 0 0
CUI: C0311262
Disease: Chronic mesenteric ischemia
Chronic mesenteric ischemia 		2 0 2 0.13 0 0
CUI: C1838230
Disease: SPINAL MUSCULAR ATROPHY, TYPE IV
SPINAL MUSCULAR ATROPHY, TYPE IV 		2 0 2 0.13 0 0
CUI: C4732793
Disease: Polyminimyoclonus
Polyminimyoclonus 		2 0 2 0.13 0 0
CUI: C0750403
Disease: Proximal weakness
Proximal weakness 		11 0 3 0.13 0 0
CUI: C0155141
Disease: Acute conjunctivitis
Acute conjunctivitis 		3 0 2 0.12 0 0
CUI: C0239548
Disease: Fasciculation, Tongue
Fasciculation, Tongue 		21 0 4 0.12 0 0
CUI: C0393546
Disease: Oculopharyngeal Spinal Muscular Atrophy
Oculopharyngeal Spinal Muscular Atrophy 		3 0 2 0.12 0 0
CUI: C0751334
Disease: Progressive Proximal Myelopathic Muscular Atrophy
Progressive Proximal Myelopathic Muscular Atrophy 		3 0 2 0.12 0 0
CUI: C0751335
Disease: Scapuloperoneal Form of Spinal Muscular Atrophy
Scapuloperoneal Form of Spinal Muscular Atrophy 		3 0 2 0.12 0 0
CUI: C1301959
Disease: Bulbar weakness
Bulbar weakness 		3 0 2 0.12 0 0
CUI: C1518715
Disease: Ovarian Fetiform Teratoma
Ovarian Fetiform Teratoma 		3 0 2 0.12 0 0
CUI: C1846566
Disease: Degeneration of the lateral corticospinal tracts
Degeneration of the lateral corticospinal tracts 		21 0 4 0.12 0 0