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 0.50 0 0
CUI: C4016882
Disease: SPASTIC PARAPLEGIA 4, MODIFIER OF
SPASTIC PARAPLEGIA 4, MODIFIER OF 		1 0 1 0.50 0 0
CUI: C4551776
Disease: RITSCHER-SCHINZEL SYNDROME 1
RITSCHER-SCHINZEL SYNDROME 1 		1 0 1 0.50 0 0
CUI: C1838192
Disease: SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder) 		2 0 1 0.33 0 0
CUI: C1853247
Disease: SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT
SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT 		2 0 1 0.33 0 0
CUI: C2931441
Disease: Hereditary spastic paralysis, infantile onset ascending
Hereditary spastic paralysis, infantile onset ascending 		2 0 1 0.33 0 0
CUI: C4025876
Disease: Abnormality of the fontanelles or cranial sutures
Abnormality of the fontanelles or cranial sutures 		2 0 1 0.33 0 0
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
Spastic paraplegia 15, autosomal recessive 		3 0 1 0.25 0 0
CUI: C2931355
Disease: Spastic paraplegia 3, autosomal dominant
Spastic paraplegia 3, autosomal dominant 		3 0 1 0.25 0 0
CUI: C0796137
Disease: 3C syndrome
3C syndrome 		4 6 1 0.20 6 0.50
CUI: C1334804
Disease: Motor Manifestations
Motor Manifestations 		5 0 1 0.17 0 0
CUI: C4025759
Disease: Abnormal mitral valve morphology
Abnormal mitral valve morphology 		5 0 1 0.17 0 0
CUI: C0431388
Disease: Microdysgenesis
Microdysgenesis 		6 0 1 0.14 0 0
CUI: C0241224
Disease: Spinal cord lesion
Spinal cord lesion 		7 0 1 0.12 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4 		7 0 1 0.12 0 0
CUI: C4022739
Disease: Abnormal neuron morphology
Abnormal neuron morphology 		8 0 1 0.11 0 0
CUI: C0393555
Disease: Pure hereditary spastic paraplegia
Pure hereditary spastic paraplegia 		9 0 1 1.0E-01 0 0
CUI: C1846017
Disease: Progressive pes cavus
Progressive pes cavus 		9 0 1 1.0E-01 0 0
CUI: C1854372
Disease: Impaired vibration sensation at ankles
Impaired vibration sensation at ankles 		9 0 1 1.0E-01 0 0
CUI: C1861443
Disease: Facial hemangioma
Facial hemangioma 		9 0 1 1.0E-01 0 0
CUI: C1846566
Disease: Degeneration of the lateral corticospinal tracts
Degeneration of the lateral corticospinal tracts 		21 0 2 9.5E-02 0 0
CUI: C0410180
Disease: Eichsfeld type congenital muscular dystrophy
Eichsfeld type congenital muscular dystrophy 		10 0 1 9.1E-02 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy 		10 0 1 9.1E-02 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 1 9.1E-02 0 0
CUI: C4025360
Disease: Functional motor deficit
Functional motor deficit 		10 0 1 9.1E-02 0 0