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: C0268632
Disease: Homocarnosinosis
Homocarnosinosis 		2 0 2 1.00 0 0
CUI: C1865864
Disease: AMYOTROPHIC LATERAL SCLEROSIS 5
AMYOTROPHIC LATERAL SCLEROSIS 5 		1 0 1 0.50 0 0
CUI: C2931821
Disease: Nakamura Osame syndrome
Nakamura Osame syndrome 		1 0 1 0.50 0 0
CUI: C3495555
Disease: Carnosinemia
Carnosinemia 		1 0 1 0.50 0 0
CUI: C4225253
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X 		1 0 1 0.50 0 0
CUI: C4324342
Disease: Dysarthrophonia
Dysarthrophonia 		1 0 1 0.50 0 0
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
Spastic paraplegia 15, autosomal recessive 		3 0 1 0.25 0 0
CUI: C4025720
Disease: Pseudobulbar behavioral symptoms
Pseudobulbar behavioral symptoms 		5 0 1 0.17 0 0
CUI: C0422837
Disease: Neurological observations
Neurological observations 		6 0 1 0.14 0 0
CUI: C0520823
Disease: Patellar clonus
Patellar clonus 		6 0 1 0.14 0 0
CUI: C0746857
Disease: Focal Neurologic Deficits
Focal Neurologic Deficits 		6 0 1 0.14 0 0
CUI: C0751377
Disease: Neurologic Dysfunction
Neurologic Dysfunction 		6 0 1 0.14 0 0
CUI: C1846564
Disease: SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE 		6 0 1 0.14 0 0
CUI: C4021582
Disease: Distal peripheral sensory neuropathy
Distal peripheral sensory neuropathy 		6 0 1 0.14 0 0
CUI: C0854078
Disease: Diabetic end stage renal disease
Diabetic end stage renal disease 		7 0 1 0.12 0 0
CUI: C1864715
Disease: Thenar muscle atrophy
Thenar muscle atrophy 		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: C0521654
Disease: Neurologic Deficits
Neurologic Deficits 		8 0 1 0.11 0 0
CUI: C0149632
Disease: Abnormality of the bladder
Abnormality of the bladder 		9 0 1 1.0E-01 0 0
CUI: C0393559
Disease: Troyer syndrome
Troyer syndrome 		9 0 1 1.0E-01 0 0
CUI: C1858479
Disease: Spastic paraplegia 11, autosomal recessive
Spastic paraplegia 11, autosomal recessive 		9 0 1 1.0E-01 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 1 9.1E-02 0 0
CUI: C1843570
Disease: Tip-toe gait
Tip-toe gait 		11 0 1 8.3E-02 0 0
CUI: C0027854
Disease: Neurologic Manifestations
Neurologic Manifestations 		12 0 1 7.7E-02 0 0
CUI: C4024949
Disease: Generalized hyperreflexia
Generalized hyperreflexia 		12 0 1 7.7E-02 0 0