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: C1847896
Disease: Charcot-Marie-Tooth Disease, Dominant Intermediate A
Charcot-Marie-Tooth Disease, Dominant Intermediate A 		2 0 2 0.22 0 0
CUI: C1837552
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder) 		3 0 2 0.20 0 0
CUI: C3888087
Disease: Charcot-Marie-Tooth disease, Type 2I
Charcot-Marie-Tooth disease, Type 2I 		4 0 2 0.18 0 0
CUI: C1853710
Disease: HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)
HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder) 		5 0 2 0.17 0 0
CUI: C1854150
Disease: Charcot-Marie-Tooth disease, Type 2B2
Charcot-Marie-Tooth disease, Type 2B2 		5 0 2 0.17 0 0
CUI: C1847823
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F 		6 0 2 0.15 0 0
CUI: C2079538
Disease: Charcot-Marie-Tooth disease, Type 2A
Charcot-Marie-Tooth disease, Type 2A 		7 0 2 0.14 0 0
CUI: C4721916
Disease: HMSN Type V
HMSN Type V 		7 0 2 0.14 0 0
CUI: C0751576
Disease: Partial Paralysis (Paresis) Vocal Cords
Partial Paralysis (Paresis) Vocal Cords 		10 0 2 0.12 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy 		10 0 2 0.12 0 0
CUI: C0264491
Disease: Acute-on-chronic respiratory failure
Acute-on-chronic respiratory failure 		1 0 1 0.11 0 0
CUI: C0339304
Disease: Neoplasm of cornea
Neoplasm of cornea 		1 0 1 0.11 0 0
CUI: C0393818
Disease: Congenital hypomyelinating neuropathy
Congenital hypomyelinating neuropathy 		11 0 2 0.11 0 0
CUI: C0750403
Disease: Proximal weakness
Proximal weakness 		11 0 2 0.11 0 0
CUI: C1167779
Disease: Neutropenic infection
Neutropenic infection 		1 0 1 0.11 0 0
CUI: C1861678
Disease: Charcot-Marie-Tooth Disease, Axonal, Type 2a1
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 		1 0 1 0.11 0 0
CUI: C1861827
Disease: Cataract, Nuclear Diffuse Nonprogressive
Cataract, Nuclear Diffuse Nonprogressive 		1 0 1 0.11 0 0
CUI: C2751831
Disease: Myopathy, Myofibrillar, Bag3-Related
Myopathy, Myofibrillar, Bag3-Related 		1 0 1 0.11 0 0
CUI: C3151293
Disease: CARDIOMYOPATHY, DILATED, 1HH
CARDIOMYOPATHY, DILATED, 1HH 		1 0 1 0.11 0 0
CUI: C4020736
Disease: Elevated urinary homovanillic acid
Elevated urinary homovanillic acid 		1 0 1 0.11 0 0
CUI: C4024821
Disease: Diffuse nuclear cataract
Diffuse nuclear cataract 		1 0 1 0.11 0 0
CUI: C1833308
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V 		12 0 2 0.11 0 0
CUI: C2931276
Disease: Spastic paraplegia 17
Spastic paraplegia 17 		12 0 2 0.11 0 0
CUI: C0000734
Disease: Abdominal mass
Abdominal mass 		2 0 1 1.0E-01 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 1.0E-01 0 0