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: C1504405
Disease: Pyramidal Tract Dysfunction
Pyramidal Tract Dysfunction 		3 0 1 0.33 0 0
CUI: C3888209
Disease: SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE 		3 0 1 0.33 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4 		7 0 1 0.14 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 1 1.0E-01 0 0
CUI: C0205711
Disease: Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher Disease 		30 0 1 3.3E-02 0 0
CUI: C0017086
Disease: Gangrene
Gangrene 		69 0 1 1.4E-02 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 8.1E-03 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 0 1 6.9E-03 0 0
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		198 0 1 5.1E-03 0 0
CUI: C1861305
Disease: TARSAL-CARPAL COALITION SYNDROME
TARSAL-CARPAL COALITION SYNDROME 		261 0 1 3.8E-03 0 0
CUI: C0011644
Disease: Scleroderma
Scleroderma 		316 0 1 3.2E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		385 0 1 2.6E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		580 0 1 1.7E-03 0 0
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		979 0 1 1.0E-03 0 0
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		1256 0 1 8.0E-04 0 0
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders 		1515 0 1 6.6E-04 0 0
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		1768 0 1 5.7E-04 0 0