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: C1865864
Disease: AMYOTROPHIC LATERAL SCLEROSIS 5
AMYOTROPHIC LATERAL SCLEROSIS 5 		1 8 1 1.00 2 0.14
CUI: C2931821
Disease: Nakamura Osame syndrome
Nakamura Osame syndrome 		1 0 1 1.00 0 0
CUI: C4324342
Disease: Dysarthrophonia
Dysarthrophonia 		1 0 1 1.00 0 0
CUI: C0268632
Disease: Homocarnosinosis
Homocarnosinosis 		2 0 1 0.50 0 0
CUI: C3495554
Disease: Homocarnosinase deficiency
Homocarnosinase deficiency 		2 0 1 0.50 0 0
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
Spastic paraplegia 15, autosomal recessive 		3 0 1 0.33 0 0
CUI: C4025720
Disease: Pseudobulbar behavioral symptoms
Pseudobulbar behavioral symptoms 		5 0 1 0.20 0 0
CUI: C0520823
Disease: Patellar clonus
Patellar clonus 		6 0 1 0.17 0 0
CUI: C1846564
Disease: SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE 		6 0 1 0.17 0 0
CUI: C4021582
Disease: Distal peripheral sensory neuropathy
Distal peripheral sensory neuropathy 		6 0 1 0.17 0 0
CUI: C1864715
Disease: Thenar muscle atrophy
Thenar muscle atrophy 		7 0 1 0.14 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4 		7 0 1 0.14 0 0
CUI: C0149632
Disease: Abnormality of the bladder
Abnormality of the bladder 		9 0 1 0.11 0 0
CUI: C0393559
Disease: Troyer syndrome
Troyer syndrome 		9 0 1 0.11 0 0
CUI: C1858479
Disease: Spastic paraplegia 11, autosomal recessive
Spastic paraplegia 11, autosomal recessive 		9 134 1 0.11 8 6.0E-02
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 1 1.0E-01 0 0
CUI: C1843570
Disease: Tip-toe gait
Tip-toe gait 		11 0 1 9.1E-02 0 0
CUI: C4024949
Disease: Generalized hyperreflexia
Generalized hyperreflexia 		12 0 1 8.3E-02 0 0
CUI: C2931356
Disease: Spastic paraplegia type 5A, recessive
Spastic paraplegia type 5A, recessive 		13 0 1 7.7E-02 0 0
CUI: C0747251
Disease: Progressive spastic paraparesis
Progressive spastic paraparesis 		14 0 1 7.1E-02 0 0
CUI: C0393556
Disease: Complicated hereditary spastic paraplegia
Complicated hereditary spastic paraplegia 		16 0 1 6.2E-02 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		20 0 1 5.0E-02 0 0
CUI: C3468114
Disease: Juvenile amyotrophic lateral sclerosis
Juvenile amyotrophic lateral sclerosis 		20 0 1 5.0E-02 0 0
CUI: C4025723
Disease: Abnormal upper motor neuron morphology
Abnormal upper motor neuron morphology 		20 0 1 5.0E-02 0 0
CUI: C0431370
Disease: Atrophy of corpus callosum
Atrophy of corpus callosum 		21 0 1 4.8E-02 0 0