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: C2673700
Disease: Brisk reflexes
Brisk reflexes 		31 7 4 9.3E-02 1 8.3E-02
CUI: C0264162
Disease: Camptocormia
Camptocormia 		8 0 2 9.1E-02 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		20 0 3 9.1E-02 0 0
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia 		21 3 3 8.8E-02 3 0.50
CUI: C0393524
Disease: Cerebellar Ataxia, Late Onset
Cerebellar Ataxia, Late Onset 		9 0 2 8.7E-02 0 0
CUI: C1837256
Disease: Macrovesicular hepatic steatosis
Macrovesicular hepatic steatosis 		9 0 2 8.7E-02 0 0
CUI: C4025573
Disease: Increased muscle fatiguability
Increased muscle fatiguability 		9 3 2 8.7E-02 1 0.12
CUI: C1389280
Disease: Basal ganglia calcification
Basal ganglia calcification 		22 0 3 8.6E-02 0 0
CUI: C1843921
Disease: Postural instability
Postural instability 		60 5 6 8.6E-02 2 0.22
CUI: C0700078
Disease: Decreased tendon reflex
Decreased tendon reflex 		10 13 2 8.3E-02 3 0.19
CUI: C1853394
Disease: Gaze-evoked horizontal nystagmus
Gaze-evoked horizontal nystagmus 		10 1 2 8.3E-02 1 0.17
CUI: C4023042
Disease: Abnormality of the mitochondrion
Abnormality of the mitochondrion 		10 0 2 8.3E-02 0 0
CUI: C0151564
Disease: Cogwheel Rigidity
Cogwheel Rigidity 		24 0 3 8.1E-02 0 0
CUI: C4476793
Disease: Abnormal cell morphology
Abnormal cell morphology 		12 0 2 7.7E-02 0 0
CUI: C0015371
Disease: Extrapyramidal Disorders
Extrapyramidal Disorders 		27 0 3 7.5E-02 0 0
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia 		27 0 3 7.5E-02 0 0
CUI: C1836842
Disease: Psychomotor deterioration
Psychomotor deterioration 		13 0 2 7.4E-02 0 0
CUI: C1849156
Disease: Spastic Ataxia
Spastic Ataxia 		28 3 3 7.3E-02 1 0.12
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity 		43 0 4 7.3E-02 0 0
CUI: C0239831
Disease: Hand muscle weakness
Hand muscle weakness 		14 1 2 7.1E-02 1 0.17
CUI: C0795878
Disease: Monosomy 22
Monosomy 22 		14 0 2 7.1E-02 0 0
CUI: C1273957
Disease: Upper limb spasticity
Upper limb spasticity 		14 0 2 7.1E-02 0 0
CUI: C1859606
Disease: Decreased number of large peripheral myelinated nerve fibers
Decreased number of large peripheral myelinated nerve fibers 		14 0 2 7.1E-02 0 0
CUI: C4024946
Disease: Focal white matter lesions
Focal white matter lesions 		14 0 2 7.1E-02 0 0
CUI: C0454596
Disease: Dysarthria, Spastic
Dysarthria, Spastic 		30 0 3 7.0E-02 0 0