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: C0443306
Disease: Spastic
Spastic 		13 0 5 0.14 0 0
CUI: C1864723
Disease: Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 		5 0 4 0.14 0 0
CUI: C0454596
Disease: Dysarthria, Spastic
Dysarthria, Spastic 		30 0 7 0.14 0 0
CUI: C0270733
Disease: Striatonigral Degeneration
Striatonigral Degeneration 		7 0 4 0.13 0 0
CUI: C1839264
Disease: SPASTIC PARAPLEGIA 2, X-LINKED (disorder)
SPASTIC PARAPLEGIA 2, X-LINKED (disorder) 		8 0 4 0.12 0 0
CUI: C0751604
Disease: Hereditary X-Linked Recessive Spastic Paraplegia
Hereditary X-Linked Recessive Spastic Paraplegia 		10 0 4 0.12 0 0
CUI: C4274084
Disease: Pelizaeus Merzbacher like disease
Pelizaeus Merzbacher like disease 		10 0 4 0.12 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		20 0 5 0.12 0 0
CUI: C0205711
Disease: Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher Disease 		30 0 6 0.12 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 41 15 0.11 1 2.3E-02
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		75 37 10 0.11 1 2.6E-02
CUI: C3554366
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q 		4 0 3 0.10 0 0
CUI: C0795953
Disease: MASA SYNDROME (disorder)
MASA SYNDROME (disorder) 		16 0 4 1.0E-01 0 0
CUI: C3711370
Disease: Spastic Paraplegia Type 7
Spastic Paraplegia Type 7 		5 2 3 1.0E-01 1 0.25
CUI: C1849134
Disease: Impaired vibration sensation in the lower limbs
Impaired vibration sensation in the lower limbs 		39 0 6 9.8E-02 0 0
CUI: C1608410
Disease: Head titubation
Head titubation 		7 0 3 9.4E-02 0 0
CUI: C0742038
Disease: Cerebellar signs
Cerebellar signs 		24 0 4 8.3E-02 0 0
CUI: C0020630
Disease: Hypophosphatasia
Hypophosphatasia 		27 0 4 7.8E-02 0 0
CUI: C0268164
Disease: Primary hyperoxaluria, type I
Primary hyperoxaluria, type I 		27 0 4 7.8E-02 0 0
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity 		43 0 5 7.6E-02 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 93 12 7.5E-02 1 1.1E-02
CUI: C1856691
Disease: Impaired proprioception
Impaired proprioception 		15 0 3 7.5E-02 0 0
CUI: C1854489
Disease: Limb dysmetria
Limb dysmetria 		16 6 3 7.3E-02 1 0.12
CUI: C0231687
Disease: Spastic gait
Spastic gait 		62 0 6 7.1E-02 0 0
CUI: C0234649
Disease: Abnormal saccadic eye movement
Abnormal saccadic eye movement 		17 0 3 7.1E-02 0 0