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: C3683791
Disease: Ataxia Neuropathy Spectrum
Ataxia Neuropathy Spectrum 		2 2 2 7.1E-02 1 7.8E-03
CUI: C4531132
Disease: Abnormal morphology of the cerebellar cortex
Abnormal morphology of the cerebellar cortex 		2 0 2 7.1E-02 0 0
CUI: C4732793
Disease: Polyminimyoclonus
Polyminimyoclonus 		2 0 2 7.1E-02 0 0
CUI: C0751870
Disease: Heredodegenerative Disorders, Nervous System
Heredodegenerative Disorders, Nervous System 		18 0 3 7.0E-02 0 0
CUI: C0949857
Disease: Mitochondrial Respiratory Chain Deficiencies
Mitochondrial Respiratory Chain Deficiencies 		49 0 5 6.9E-02 0 0
CUI: C0032586
Disease: Polyradiculopathy
Polyradiculopathy 		3 0 2 6.9E-02 0 0
CUI: C0043116
Disease: HMN (Hereditary Motor Neuropathy) Proximal Type I
HMN (Hereditary Motor Neuropathy) Proximal Type I 		34 0 4 6.9E-02 0 0
CUI: C0155141
Disease: Acute conjunctivitis
Acute conjunctivitis 		3 0 2 6.9E-02 0 0
CUI: C0270951
Disease: Ocular muscular dystrophy
Ocular muscular dystrophy 		3 0 2 6.9E-02 0 0
CUI: C0345200
Disease: Congenital dysmotility of small intestine
Congenital dysmotility of small intestine 		3 0 2 6.9E-02 0 0
CUI: C0393546
Disease: Oculopharyngeal Spinal Muscular Atrophy
Oculopharyngeal Spinal Muscular Atrophy 		3 0 2 6.9E-02 0 0
CUI: C0751334
Disease: Progressive Proximal Myelopathic Muscular Atrophy
Progressive Proximal Myelopathic Muscular Atrophy 		3 0 2 6.9E-02 0 0
CUI: C0751335
Disease: Scapuloperoneal Form of Spinal Muscular Atrophy
Scapuloperoneal Form of Spinal Muscular Atrophy 		3 0 2 6.9E-02 0 0
CUI: C1301959
Disease: Bulbar weakness
Bulbar weakness 		3 0 2 6.9E-02 0 0
CUI: C1518715
Disease: Ovarian Fetiform Teratoma
Ovarian Fetiform Teratoma 		3 0 2 6.9E-02 0 0
CUI: C1843859
Disease: Sensory ataxic neuropathy
Sensory ataxic neuropathy 		3 0 2 6.9E-02 0 0
CUI: C3826237
Disease: Head--Tumors
Head--Tumors 		3 0 2 6.9E-02 0 0
CUI: C4024911
Disease: Acute infantile spinal muscular atrophy
Acute infantile spinal muscular atrophy 		3 0 2 6.9E-02 0 0
CUI: C4476616
Disease: Atrophic muscularis propria
Atrophic muscularis propria 		3 0 2 6.9E-02 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis 		19 0 3 6.8E-02 0 0
CUI: C0240991
Disease: Ataxia, Sensory
Ataxia, Sensory 		35 1 4 6.8E-02 1 7.8E-03
CUI: C0271682
Disease: Mixed sensory-motor polyneuropathy
Mixed sensory-motor polyneuropathy 		20 0 3 6.7E-02 0 0
CUI: C0349390
Disease: Non-fluent aphasia
Non-fluent aphasia 		4 0 2 6.7E-02 0 0
CUI: C0872218
Disease: MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME
MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME 		4 0 2 6.7E-02 0 0
CUI: C1837728
Disease: AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder) 		4 0 2 6.7E-02 0 0