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: C0442874
Disease: Neuropathy
Neuropathy 		484 110 96 0.16 20 8.8E-02
CUI: C0751036
Disease: Hereditary Motor and Sensory Neuropathy Type I
Hereditary Motor and Sensory Neuropathy Type I 		19 84 19 9.1E-02 20 1.0E-01
CUI: C0270912
Disease: Charcot-Marie-Tooth Disease, Type Ib
Charcot-Marie-Tooth Disease, Type Ib 		12 51 12 5.8E-02 11 6.2E-02
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder) 		176 45 30 8.5E-02 10 5.8E-02
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 144 35 0.16 9 3.3E-02
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		14 77 13 6.2E-02 8 3.9E-02
CUI: C1842983
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K 		2 17 2 9.6E-03 7 4.8E-02
CUI: C1859198
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder) 		3 22 3 1.4E-02 7 4.6E-02
CUI: C0027868
Disease: Neuromuscular Diseases
Neuromuscular Diseases 		171 50 31 8.9E-02 6 3.3E-02
CUI: C4721453
Disease: Peripheral Nervous System Diseases
Peripheral Nervous System Diseases 		549 69 93 0.14 6 3.0E-02
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy 		351 81 77 0.16 5 2.4E-02
CUI: C1843225
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder) 		1 16 1 4.8E-03 5 3.4E-02
CUI: C4015349
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S 		1 32 1 4.8E-03 5 3.1E-02
CUI: C0393808
Disease: Charcot-Marie-Tooth disease, X-linked, 1
Charcot-Marie-Tooth disease, X-linked, 1 		10 82 8 3.8E-02 4 1.9E-02
CUI: C0393818
Disease: Congenital hypomyelinating neuropathy
Congenital hypomyelinating neuropathy 		11 10 7 3.3E-02 4 2.8E-02
CUI: C0751335
Disease: Scapuloperoneal Form of Spinal Muscular Atrophy
Scapuloperoneal Form of Spinal Muscular Atrophy 		3 5 3 1.4E-02 4 2.9E-02
CUI: C1847823
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F 		6 15 6 2.9E-02 4 2.7E-02
CUI: C1853710
Disease: HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)
HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder) 		5 13 4 1.9E-02 4 2.8E-02
CUI: C1858517
Disease: SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1
SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1 		10 49 4 1.9E-02 4 2.2E-02
CUI: C4721887
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A 		1 21 1 4.8E-03 4 2.6E-02
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		53 11 37 0.17 3 2.1E-02
CUI: C0033300
Disease: Progeria
Progeria 		118 41 4 1.2E-02 3 1.7E-02
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		26 5 26 0.12 3 2.2E-02
CUI: C0235025
Disease: Peripheral motor neuropathy
Peripheral motor neuropathy 		64 20 30 0.12 3 2.0E-02
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		42 24 25 0.11 3 1.9E-02