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: C0042928
Disease: Vocal Cord Paralysis
Vocal Cord Paralysis 		42 0 6 0.11 0 0
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		208 0 21 0.10 0 0
CUI: C0474520
Disease: Myokymia, Generalized
Myokymia, Generalized 		2 0 2 9.5E-02 0 0
CUI: C1843183
Disease: Charcot-Marie-Tooth disease, Type 4A, axonal form
Charcot-Marie-Tooth disease, Type 4A, axonal form 		2 0 2 9.5E-02 0 0
CUI: C1861675
Disease: Cold-induced muscle cramps
Cold-induced muscle cramps 		2 0 2 9.5E-02 0 0
CUI: C4016264
Disease: DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT 		2 0 2 9.5E-02 0 0
CUI: C4721436
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE
NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE 		2 0 2 9.5E-02 0 0
CUI: C1806780
Disease: Increased CSF protein
Increased CSF protein 		26 0 4 9.3E-02 0 0
CUI: C0878575
Disease: Peripheral demyelination
Peripheral demyelination 		27 0 4 9.1E-02 0 0
CUI: C1854154
Disease: Charcot-Marie-Tooth disease, Type 2B1
Charcot-Marie-Tooth disease, Type 2B1 		3 0 2 9.1E-02 0 0
CUI: C1858278
Disease: Charcot-Marie-Tooth disease, Type 4B2
Charcot-Marie-Tooth disease, Type 4B2 		3 0 2 9.1E-02 0 0
CUI: C1866637
Disease: Basal lamina onion bulb formation
Basal lamina onion bulb formation 		3 0 2 9.1E-02 0 0
CUI: C2750090
Disease: Charcot-Marie-Tooth Disease, Axonal, Type 2n
Charcot-Marie-Tooth Disease, Axonal, Type 2n 		3 0 2 9.1E-02 0 0
CUI: C0393541
Disease: Distal Spinal Muscular Atrophy
Distal Spinal Muscular Atrophy 		16 0 3 8.8E-02 0 0
CUI: C1832338
Disease: Axonal loss
Axonal loss 		16 0 3 8.8E-02 0 0
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		116 0 11 8.7E-02 0 0
CUI: C1832342
Disease: Talipes cavus equinovarus
Talipes cavus equinovarus 		4 0 2 8.7E-02 0 0
CUI: C1859200
Disease: Inability to walk by childhood/adolescence
Inability to walk by childhood/adolescence 		4 0 2 8.7E-02 0 0
CUI: C3888087
Disease: Charcot-Marie-Tooth disease, Type 2I
Charcot-Marie-Tooth disease, Type 2I 		4 0 2 8.7E-02 0 0
CUI: C1854510
Disease: Abnormality of the cranial nerves
Abnormality of the cranial nerves 		17 0 3 8.6E-02 0 0
CUI: C0027743
Disease: Nerve compression syndrome
Nerve compression syndrome 		5 0 2 8.3E-02 0 0
CUI: C0558844
Disease: Knee reflex absent
Knee reflex absent 		5 0 2 8.3E-02 0 0
CUI: C1510429
Disease: Entrapment Neuropathies
Entrapment Neuropathies 		5 0 2 8.3E-02 0 0
CUI: C1832399
Disease: Charcot-Marie-Tooth disease, Type 4B1
Charcot-Marie-Tooth disease, Type 4B1 		5 0 2 8.3E-02 0 0
CUI: C1853710
Disease: HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)
HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder) 		5 0 2 8.3E-02 0 0