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: C0152227
Disease: Excessive tearing
Excessive tearing 		26 0 3 6.5E-02 0 0
CUI: C0271390
Disease: Nystagmus, End-Position
Nystagmus, End-Position 		26 0 3 6.5E-02 0 0
CUI: C1853767
Disease: Impaired distal vibration sensation
Impaired distal vibration sensation 		10 0 2 6.5E-02 0 0
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 0 7 6.4E-02 0 0
CUI: C1849156
Disease: Spastic Ataxia
Spastic Ataxia 		28 0 3 6.2E-02 0 0
CUI: C4012790
Disease: Ataxia-Telangiectasisa-Like Disorder 1
Ataxia-Telangiectasisa-Like Disorder 1 		11 0 2 6.2E-02 0 0
CUI: C0338508
Disease: Optic Atrophy 1
Optic Atrophy 1 		117 0 8 6.1E-02 0 0
CUI: C1263858
Disease: Muscular dystrophy congenital, merosin negative
Muscular dystrophy congenital, merosin negative 		12 0 2 6.1E-02 0 0
CUI: C1858391
Disease: ATAXIA-TELANGIECTASIA-LIKE DISORDER
ATAXIA-TELANGIECTASIA-LIKE DISORDER 		12 0 2 6.1E-02 0 0
CUI: C3542021
Disease: Duchenne and Becker Muscular Dystrophy
Duchenne and Becker Muscular Dystrophy 		12 0 2 6.1E-02 0 0
CUI: C0234979
Disease: Dysdiadochokinesis
Dysdiadochokinesis 		49 0 4 5.9E-02 0 0
CUI: C1861736
Disease: SPINOCEREBELLAR ATAXIA 31 (disorder)
SPINOCEREBELLAR ATAXIA 31 (disorder) 		13 0 2 5.9E-02 0 0
CUI: C4551521
Disease: Kinetic tremor
Kinetic tremor 		13 0 2 5.9E-02 0 0
CUI: C0162674
Disease: Chronic progressive external ophthalmoplegia
Chronic progressive external ophthalmoplegia 		50 0 4 5.8E-02 0 0
CUI: C1852373
Disease: Mitochondrial encephalopathy
Mitochondrial encephalopathy 		32 0 3 5.8E-02 0 0
CUI: C0162672
Disease: MERRF Syndrome
MERRF Syndrome 		51 0 4 5.7E-02 0 0
CUI: C0221261
Disease: Koilonychia
Koilonychia 		14 0 2 5.7E-02 0 0
CUI: C0239831
Disease: Hand muscle weakness
Hand muscle weakness 		14 0 2 5.7E-02 0 0
CUI: C0410173
Disease: Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder) 		14 0 2 5.7E-02 0 0
CUI: C0085543
Disease: Epilepsia Partialis Continua
Epilepsia Partialis Continua 		15 0 2 5.6E-02 0 0
CUI: C1849148
Disease: Decreased sensory nerve conduction velocity
Decreased sensory nerve conduction velocity 		15 0 2 5.6E-02 0 0
CUI: C1856691
Disease: Impaired proprioception
Impaired proprioception 		15 0 2 5.6E-02 0 0
CUI: C0751783
Disease: Lafora Disease
Lafora Disease 		92 0 6 5.5E-02 0 0
CUI: C0023003
Disease: Langer-Giedion Syndrome
Langer-Giedion Syndrome 		16 0 2 5.4E-02 0 0
CUI: C1854489
Disease: Limb dysmetria
Limb dysmetria 		16 0 2 5.4E-02 0 0