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: C3150972
Disease: NEUROPATHY, HEREDITARY SENSORY, TYPE ID
NEUROPATHY, HEREDITARY SENSORY, TYPE ID 		1 0 1 1.0E-01 0 0
CUI: C3553656
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB 		1 0 1 1.0E-01 0 0
CUI: C4016882
Disease: SPASTIC PARAPLEGIA 4, MODIFIER OF
SPASTIC PARAPLEGIA 4, MODIFIER OF 		1 1 1 1.0E-01 1 9.9E-03
CUI: C4025809
Disease: Penetrating foot ulcers
Penetrating foot ulcers 		1 0 1 1.0E-01 0 0
CUI: C4225253
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X 		1 0 1 1.0E-01 0 0
CUI: C4324342
Disease: Dysarthrophonia
Dysarthrophonia 		1 0 1 1.0E-01 0 0
CUI: C4553976
Disease: Urinary Urgency, CTCAE 5
Urinary Urgency, CTCAE 5 		34 0 4 1.0E-01 0 0
CUI: C2931356
Disease: Spastic paraplegia type 5A, recessive
Spastic paraplegia type 5A, recessive 		13 0 2 9.5E-02 0 0
CUI: C0268632
Disease: Homocarnosinosis
Homocarnosinosis 		2 0 1 9.1E-02 0 0
CUI: C0747251
Disease: Progressive spastic paraparesis
Progressive spastic paraparesis 		14 0 2 9.1E-02 0 0
CUI: C1833222
Disease: Autoamputation
Autoamputation 		2 0 1 9.1E-02 0 0
CUI: C1863704
Disease: Spastic paraplegia 8, autosomal dominant
Spastic paraplegia 8, autosomal dominant 		2 0 1 9.1E-02 0 0
CUI: C1970009
Disease: SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE 		2 0 1 9.1E-02 0 0
CUI: C2931441
Disease: Hereditary spastic paralysis, infantile onset ascending
Hereditary spastic paralysis, infantile onset ascending 		2 15 1 9.1E-02 1 8.7E-03
CUI: C3495554
Disease: Homocarnosinase deficiency
Homocarnosinase deficiency 		2 0 1 9.1E-02 0 0
CUI: C4023800
Disease: Limitation of movement at ankles
Limitation of movement at ankles 		2 0 1 9.1E-02 0 0
CUI: C1849134
Disease: Impaired vibration sensation in the lower limbs
Impaired vibration sensation in the lower limbs 		39 0 4 8.9E-02 0 0
CUI: C0013608
Disease: Edema, Cardiac
Edema, Cardiac 		3 0 1 8.3E-02 0 0
CUI: C1832276
Disease: Thenar muscle weakness
Thenar muscle weakness 		3 0 1 8.3E-02 0 0
CUI: C1832277
Disease: First dorsal interossei muscle weakness
First dorsal interossei muscle weakness 		3 0 1 8.3E-02 0 0
CUI: C1832278
Disease: First dorsal interossei muscle atrophy
First dorsal interossei muscle atrophy 		3 0 1 8.3E-02 0 0
CUI: C1832279
Disease: Cold-induced hand cramps
Cold-induced hand cramps 		3 0 1 8.3E-02 0 0
CUI: C1843175
Disease: Hyperreflexia in upper limbs
Hyperreflexia in upper limbs 		16 0 2 8.3E-02 0 0
CUI: C1848745
Disease: Oliver-McFarlane syndrome
Oliver-McFarlane syndrome 		3 0 1 8.3E-02 0 0
CUI: C1864975
Disease: Osteomyelitis leading to amputation due to slow healing fractures
Osteomyelitis leading to amputation due to slow healing fractures 		3 0 1 8.3E-02 0 0