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: C4025696
Disease: Paresis of extensor muscles of the big toe
Paresis of extensor muscles of the big toe 		4 0 2 0.22 0 0
CUI: C1854023
Disease: Spinal muscular atrophy, Jerash type
Spinal muscular atrophy, Jerash type 		5 0 2 0.20 0 0
CUI: C4021578
Disease: Chronic axonal neuropathy
Chronic axonal neuropathy 		5 0 2 0.20 0 0
CUI: C3661519
Disease: Hereditary Motor Neuronopathy
Hereditary Motor Neuronopathy 		12 0 3 0.19 0 0
CUI: C1847823
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F 		6 0 2 0.18 0 0
CUI: C1849096
Disease: Infantile onset spinocerebellar ataxia
Infantile onset spinocerebellar ataxia 		6 0 2 0.18 0 0
CUI: C0234366
Disease: Ataxic
Ataxic 		15 0 3 0.16 0 0
CUI: C3711384
Disease: Distal Hereditary Motor Neuropathy, Type II
Distal Hereditary Motor Neuropathy, Type II 		8 0 2 0.15 0 0
CUI: C0558193
Disease: Stiff limbs
Stiff limbs 		1 0 1 0.14 0 0
CUI: C0576690
Disease: Impaired body position sense
Impaired body position sense 		1 0 1 0.14 0 0
CUI: C1834692
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA 		1 0 1 0.14 0 0
CUI: C1836439
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 		1 0 1 0.14 0 0
CUI: C1842026
Disease: GLAUCOMA 1, OPEN ANGLE, E
GLAUCOMA 1, OPEN ANGLE, E 		1 0 1 0.14 0 0
CUI: C1865416
Disease: Pallor of dorsal columns of the spinal cord
Pallor of dorsal columns of the spinal cord 		1 0 1 0.14 0 0
CUI: C2608087
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB 		1 0 1 0.14 0 0
CUI: C3150692
Disease: AMYOTROPHIC LATERAL SCLEROSIS 12
AMYOTROPHIC LATERAL SCLEROSIS 12 		1 0 1 0.14 0 0
CUI: C4015307
Disease: PERRAULT SYNDROME 5
PERRAULT SYNDROME 5 		1 0 1 0.14 0 0
CUI: C4509818
Disease: Facial onset sensory and motor neuronopathy syndrome
Facial onset sensory and motor neuronopathy syndrome 		1 0 1 0.14 0 0
CUI: C1853767
Disease: Impaired distal vibration sensation
Impaired distal vibration sensation 		10 0 2 0.13 0 0
CUI: C0035066
Disease: Renal Artery Obstruction
Renal Artery Obstruction 		2 0 1 0.12 0 0
CUI: C0270942
Disease: Myasthenic crisis
Myasthenic crisis 		2 0 1 0.12 0 0
CUI: C1282365
Disease: Mixed type cataract
Mixed type cataract 		2 0 1 0.12 0 0
CUI: C1843858
Disease: Atrophy/Degeneration involving the spinal cord
Atrophy/Degeneration involving the spinal cord 		2 0 1 0.12 0 0
CUI: C1847730
Disease: GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO (finding)
GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO (finding) 		2 0 1 0.12 0 0
CUI: C1862940
Disease: Amyotrophic Lateral Sclerosis, Autosomal Recessive
Amyotrophic Lateral Sclerosis, Autosomal Recessive 		2 0 1 0.12 0 0