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: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 0 5 9.4E-02 0 0
CUI: C0393808
Disease: Charcot-Marie-Tooth disease, X-linked, 1
Charcot-Marie-Tooth disease, X-linked, 1 		10 0 5 9.4E-02 0 0
CUI: C0393818
Disease: Congenital hypomyelinating neuropathy
Congenital hypomyelinating neuropathy 		11 0 5 9.3E-02 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 30 9.1E-02 0 0
CUI: C0027889
Disease: Hereditary Sensory and Autonomic Neuropathies
Hereditary Sensory and Autonomic Neuropathies 		25 0 6 9.0E-02 0 0
CUI: C0151572
Disease: Reflex, Corneal, Decreased
Reflex, Corneal, Decreased 		14 0 5 8.8E-02 0 0
CUI: C0917990
Disease: Acro-Osteolysis
Acro-Osteolysis 		16 0 5 8.5E-02 0 0
CUI: C1858712
Disease: Spastic paraplegia 10, autosomal dominant
Spastic paraplegia 10, autosomal dominant 		16 0 5 8.5E-02 0 0
CUI: C0042928
Disease: Vocal Cord Paralysis
Vocal Cord Paralysis 		42 0 7 8.4E-02 0 0
CUI: C0587246
Disease: Muscle weakness of limb
Muscle weakness of limb 		42 0 7 8.4E-02 0 0
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy 		351 81 31 8.4E-02 1 4.5E-03
CUI: C3888087
Disease: Charcot-Marie-Tooth disease, Type 2I
Charcot-Marie-Tooth disease, Type 2I 		4 14 4 8.3E-02 1 6.4E-03
CUI: C4025619
Disease: Peripheral axonal atrophy
Peripheral axonal atrophy 		4 0 4 8.3E-02 0 0
CUI: C1833225
Disease: Dystrophic toenail
Dystrophic toenail 		18 0 5 8.2E-02 0 0
CUI: C4025614
Disease: EMG: chronic denervation signs
EMG: chronic denervation signs 		18 0 5 8.2E-02 0 0
CUI: C1853710
Disease: HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)
HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder) 		5 0 4 8.2E-02 0 0
CUI: C2752089
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIA
Neuropathy, Hereditary Sensory And Autonomic, Type IIA 		5 0 4 8.2E-02 0 0
CUI: C0728829
Disease: Congenital pes cavus
Congenital pes cavus 		19 0 5 8.1E-02 0 0
CUI: C0151934
Disease: Hypogeusia
Hypogeusia 		6 0 4 8.0E-02 0 0
CUI: C4025744
Disease: Foot acroosteolysis
Foot acroosteolysis 		6 0 4 8.0E-02 0 0
CUI: C0271682
Disease: Mixed sensory-motor polyneuropathy
Mixed sensory-motor polyneuropathy 		20 0 5 7.9E-02 0 0
CUI: C1857171
Disease: Episodic hyperhidrosis
Episodic hyperhidrosis 		20 0 5 7.9E-02 0 0
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder) 		176 0 16 7.7E-02 0 0
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		8 0 4 7.7E-02 0 0
CUI: C0442874
Disease: Neuropathy
Neuropathy 		484 110 38 7.7E-02 2 7.9E-03