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 0.25 0 0
CUI: C1836485
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder) 		1 0 1 0.25 0 0
CUI: C1842197
Disease: Charcot-Marie-Tooth Disease, Recessive Intermediate A
Charcot-Marie-Tooth Disease, Recessive Intermediate A 		1 0 1 0.25 0 0
CUI: C1842984
Disease: Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k
Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k 		1 0 1 0.25 0 0
CUI: C3554182
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15 		1 11 1 0.25 1 8.3E-02
CUI: C4013993
Disease: Bilateral striatal necrosis
Bilateral striatal necrosis 		1 1 1 0.25 1 0.50
CUI: C4016973
Disease: NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE
NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE 		1 0 1 0.25 0 0
CUI: C4225351
Disease: White Sutton syndrome
White Sutton syndrome 		1 0 1 0.25 0 0
CUI: C4310725
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B 		1 0 1 0.25 0 0
CUI: C4310875
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2A
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2A 		1 0 1 0.25 0 0
CUI: C4318382
Disease: Cardiac Conduction Defects
Cardiac Conduction Defects 		1 1 1 0.25 1 0.50
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 0.25 0 0
CUI: C4721887
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A 		1 0 1 0.25 0 0
CUI: C4748826
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27 		1 2 1 0.25 1 0.33
CUI: C1842983
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K 		2 0 1 0.20 0 0
CUI: C1843183
Disease: Charcot-Marie-Tooth disease, Type 4A, axonal form
Charcot-Marie-Tooth disease, Type 4A, axonal form 		2 0 1 0.20 0 0
CUI: C1968790
Disease: Axonal degeneration/regeneration
Axonal degeneration/regeneration 		8 0 2 0.20 0 0
CUI: C0751576
Disease: Partial Paralysis (Paresis) Vocal Cords
Partial Paralysis (Paresis) Vocal Cords 		10 0 2 0.17 0 0
CUI: C1859198
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder) 		3 0 1 0.17 0 0
CUI: C1866637
Disease: Basal lamina onion bulb formation
Basal lamina onion bulb formation 		3 0 1 0.17 0 0
CUI: C0040435
Disease: Tooth Diseases
Tooth Diseases 		4 0 1 0.14 0 0
CUI: C4025619
Disease: Peripheral axonal atrophy
Peripheral axonal atrophy 		4 0 1 0.14 0 0
CUI: C4025696
Disease: Paresis of extensor muscles of the big toe
Paresis of extensor muscles of the big toe 		4 0 1 0.14 0 0
CUI: C4025722
Disease: Abnormality of the spinal cord
Abnormality of the spinal cord 		4 0 1 0.14 0 0
CUI: C0558844
Disease: Knee reflex absent
Knee reflex absent 		5 0 1 0.12 0 0