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: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria 		1 0 1 0.33 0 0
CUI: C1865864
Disease: AMYOTROPHIC LATERAL SCLEROSIS 5
AMYOTROPHIC LATERAL SCLEROSIS 5 		1 0 1 0.33 0 0
CUI: C2931821
Disease: Nakamura Osame syndrome
Nakamura Osame syndrome 		1 0 1 0.33 0 0
CUI: C4016882
Disease: SPASTIC PARAPLEGIA 4, MODIFIER OF
SPASTIC PARAPLEGIA 4, MODIFIER OF 		1 0 1 0.33 0 0
CUI: C4225253
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X 		1 0 1 0.33 0 0
CUI: C4293685
Disease: Deep cerebral white matter hyperdensities
Deep cerebral white matter hyperdensities 		1 0 1 0.33 0 0
CUI: C4324342
Disease: Dysarthrophonia
Dysarthrophonia 		1 0 1 0.33 0 0
CUI: C0268632
Disease: Homocarnosinosis
Homocarnosinosis 		2 0 1 0.25 0 0
CUI: C1838192
Disease: SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder) 		2 0 1 0.25 0 0
CUI: C1853247
Disease: SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT
SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT 		2 0 1 0.25 0 0
CUI: C1863704
Disease: Spastic paraplegia 8, autosomal dominant
Spastic paraplegia 8, autosomal dominant 		2 0 1 0.25 0 0
CUI: C2675186
Disease: LEBER CONGENITAL AMAUROSIS 13
LEBER CONGENITAL AMAUROSIS 13 		2 0 1 0.25 0 0
CUI: C2931441
Disease: Hereditary spastic paralysis, infantile onset ascending
Hereditary spastic paralysis, infantile onset ascending 		2 0 1 0.25 0 0
CUI: C3495554
Disease: Homocarnosinase deficiency
Homocarnosinase deficiency 		2 0 1 0.25 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4 		7 0 2 0.25 0 0
CUI: C0393559
Disease: Troyer syndrome
Troyer syndrome 		9 0 2 0.20 0 0
CUI: C1858479
Disease: Spastic paraplegia 11, autosomal recessive
Spastic paraplegia 11, autosomal recessive 		9 0 2 0.20 0 0
CUI: C2931355
Disease: Spastic paraplegia 3, autosomal dominant
Spastic paraplegia 3, autosomal dominant 		3 0 1 0.20 0 0
CUI: C3806583
Disease: Functional abnormality of the bladder
Functional abnormality of the bladder 		3 0 1 0.20 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 2 0.18 0 0
CUI: C1843570
Disease: Tip-toe gait
Tip-toe gait 		11 0 2 0.17 0 0
CUI: C0423414
Disease: Retinal flecking
Retinal flecking 		5 0 1 0.14 0 0
CUI: C1334804
Disease: Motor Manifestations
Motor Manifestations 		5 0 1 0.14 0 0
CUI: C4024610
Disease: Leg muscle stiffness
Leg muscle stiffness 		13 0 2 0.14 0 0
CUI: C4025720
Disease: Pseudobulbar behavioral symptoms
Pseudobulbar behavioral symptoms 		5 0 1 0.14 0 0