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: C0016512
Disease: Foot pain
Foot pain 		1 0 1 1.00 0 0
CUI: C1836485
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder) 		1 0 1 1.00 0 0
CUI: C4310875
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2A
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2A 		1 0 1 1.00 0 0
CUI: C4707897
Disease: Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
Severe early-onset axonal neuropathy due to mitofusin 2 deficiency 		1 0 1 1.00 0 0
CUI: C4721887
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A 		1 21 1 1.00 4 0.15
CUI: C1859200
Disease: Inability to walk by childhood/adolescence
Inability to walk by childhood/adolescence 		4 0 1 0.25 0 0
CUI: C4025619
Disease: Peripheral axonal atrophy
Peripheral axonal atrophy 		4 0 1 0.25 0 0
CUI: C4025696
Disease: Paresis of extensor muscles of the big toe
Paresis of extensor muscles of the big toe 		4 0 1 0.25 0 0
CUI: C4025722
Disease: Abnormality of the spinal cord
Abnormality of the spinal cord 		4 0 1 0.25 0 0
CUI: C0558844
Disease: Knee reflex absent
Knee reflex absent 		5 0 1 0.20 0 0
CUI: C1850854
Disease: Increased laxity of ankles
Increased laxity of ankles 		5 0 1 0.20 0 0
CUI: C0393807
Disease: Hereditary motor and sensory neuropathy with optic atrophy (disorder)
Hereditary motor and sensory neuropathy with optic atrophy (disorder) 		7 11 1 0.14 4 0.24
CUI: C1328349
Disease: Neuropathy ataxia and retinis pigmentosa
Neuropathy ataxia and retinis pigmentosa 		7 0 1 0.14 0 0
CUI: C2079538
Disease: Charcot-Marie-Tooth disease, Type 2A
Charcot-Marie-Tooth disease, Type 2A 		7 3 1 0.14 1 8.3E-02
CUI: C4721916
Disease: HMSN Type V
HMSN Type V 		7 0 1 0.14 0 0
CUI: C1262113
Disease: Lipohypertrophy
Lipohypertrophy 		8 0 1 0.12 0 0
CUI: C1968790
Disease: Axonal degeneration/regeneration
Axonal degeneration/regeneration 		8 0 1 0.12 0 0
CUI: C4021222
Disease: Impaired temperature sensation
Impaired temperature sensation 		8 0 1 0.12 0 0
CUI: C0392553
Disease: Hereditary peripheral neuropathy
Hereditary peripheral neuropathy 		9 0 1 0.11 0 0
CUI: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy 		9 0 1 0.11 0 0
CUI: C1836527
Disease: Distal sensory impairment of all modalities
Distal sensory impairment of all modalities 		9 0 1 0.11 0 0
CUI: C0239377
Disease: Arm Pain
Arm Pain 		10 0 1 1.0E-01 0 0
CUI: C0279746
Disease: Adenocarcinoma of salivary gland
Adenocarcinoma of salivary gland 		10 0 1 1.0E-01 0 0
CUI: C0751576
Disease: Partial Paralysis (Paresis) Vocal Cords
Partial Paralysis (Paresis) Vocal Cords 		10 0 1 1.0E-01 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3 		12 0 1 8.3E-02 0 0