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: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy 		9 0 4 0.19 0 0
CUI: C0393546
Disease: Oculopharyngeal Spinal Muscular Atrophy
Oculopharyngeal Spinal Muscular Atrophy 		3 0 3 0.19 0 0
CUI: C0751334
Disease: Progressive Proximal Myelopathic Muscular Atrophy
Progressive Proximal Myelopathic Muscular Atrophy 		3 0 3 0.19 0 0
CUI: C0751335
Disease: Scapuloperoneal Form of Spinal Muscular Atrophy
Scapuloperoneal Form of Spinal Muscular Atrophy 		3 0 3 0.19 0 0
CUI: C2931358
Disease: Muscular atrophy, spinal, infantile chronic form
Muscular atrophy, spinal, infantile chronic form 		4 0 3 0.18 0 0
CUI: C0750403
Disease: Proximal weakness
Proximal weakness 		11 0 4 0.17 0 0
CUI: C1833308
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V 		12 0 4 0.17 0 0
CUI: C1853710
Disease: HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)
HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder) 		5 13 3 0.17 1 5.0E-02
CUI: C2931276
Disease: Spastic paraplegia 17
Spastic paraplegia 17 		12 0 4 0.17 0 0
CUI: C3661519
Disease: Hereditary Motor Neuronopathy
Hereditary Motor Neuronopathy 		12 0 4 0.17 0 0
CUI: C0393538
Disease: Muscular Atrophy, Spinal, Type II
Muscular Atrophy, Spinal, Type II 		6 0 3 0.16 0 0
CUI: C0700595
Disease: Spinal Muscular Atrophies of Childhood
Spinal Muscular Atrophies of Childhood 		6 0 3 0.16 0 0
CUI: C4750288
Disease: Spinal muscular atrophy with lower extremity predominance
Spinal muscular atrophy with lower extremity predominance 		6 0 3 0.16 0 0
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy 		14 0 4 0.15 0 0
CUI: C0270765
Disease: Myelopathic Muscular Atrophy
Myelopathic Muscular Atrophy 		7 0 3 0.15 0 0
CUI: C0393547
Disease: Bulbospinal Neuronopathy
Bulbospinal Neuronopathy 		7 0 3 0.15 0 0
CUI: C1843505
Disease: Degeneration of anterior horn cells
Degeneration of anterior horn cells 		15 0 4 0.15 0 0
CUI: C1865384
Disease: Amyotrophy, monomelic
Amyotrophy, monomelic 		15 0 4 0.15 0 0
CUI: C0154681
Disease: Anterior Horn Cell Disease
Anterior Horn Cell Disease 		8 0 3 0.14 0 0
CUI: C0751576
Disease: Partial Paralysis (Paresis) Vocal Cords
Partial Paralysis (Paresis) Vocal Cords 		10 0 3 0.13 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy 		10 0 3 0.13 0 0
CUI: C1858517
Disease: SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1
SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1 		10 49 3 0.13 1 1.8E-02
CUI: C4021727
Disease: EMG: neuropathic changes
EMG: neuropathic changes 		28 0 5 0.13 0 0
CUI: C0038828
Disease: Superior Mesenteric Artery Syndrome
Superior Mesenteric Artery Syndrome 		2 0 2 0.12 0 0
CUI: C0311262
Disease: Chronic mesenteric ischemia
Chronic mesenteric ischemia 		2 0 2 0.12 0 0