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: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		75 0 9 9.7E-02 0 0
CUI: C0393807
Disease: Hereditary motor and sensory neuropathy with optic atrophy (disorder)
Hereditary motor and sensory neuropathy with optic atrophy (disorder) 		7 0 3 9.7E-02 0 0
CUI: C2079538
Disease: Charcot-Marie-Tooth disease, Type 2A
Charcot-Marie-Tooth disease, Type 2A 		7 0 3 9.7E-02 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4 		7 0 3 9.7E-02 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies 		104 0 11 9.2E-02 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense 		33 0 5 9.1E-02 0 0
CUI: C1854372
Disease: Impaired vibration sensation at ankles
Impaired vibration sensation at ankles 		9 0 3 9.1E-02 0 0
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy 		94 0 10 9.0E-02 0 0
CUI: C0751576
Disease: Partial Paralysis (Paresis) Vocal Cords
Partial Paralysis (Paresis) Vocal Cords 		10 0 3 8.8E-02 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy 		10 0 3 8.8E-02 0 0
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		198 59 18 8.7E-02 4 6.5E-02
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		23 0 4 8.7E-02 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3 		12 0 3 8.3E-02 0 0
CUI: C1833308
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V 		12 0 3 8.3E-02 0 0
CUI: C2931356
Disease: Spastic paraplegia type 5A, recessive
Spastic paraplegia type 5A, recessive 		13 0 3 8.1E-02 0 0
CUI: C4024610
Disease: Leg muscle stiffness
Leg muscle stiffness 		13 0 3 8.1E-02 0 0
CUI: C0239831
Disease: Hand muscle weakness
Hand muscle weakness 		14 0 3 7.9E-02 0 0
CUI: C1273957
Disease: Upper limb spasticity
Upper limb spasticity 		14 0 3 7.9E-02 0 0
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy 		14 0 3 7.9E-02 0 0
CUI: C3276549
Disease: OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY 		14 0 3 7.9E-02 0 0
CUI: C0030486
Disease: Paraplegia
Paraplegia 		59 0 6 7.5E-02 0 0
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy 		59 0 6 7.5E-02 0 0
CUI: C0393556
Disease: Complicated hereditary spastic paraplegia
Complicated hereditary spastic paraplegia 		16 0 3 7.5E-02 0 0
CUI: C1854489
Disease: Limb dysmetria
Limb dysmetria 		16 0 3 7.5E-02 0 0
CUI: C1721053
Disease: Female Athlete Triad Syndrome
Female Athlete Triad Syndrome 		2 0 2 7.4E-02 0 0