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: C4022737
Disease: Neurodevelopmental abnormality
Neurodevelopmental abnormality 		7 0 1 9.1E-02 0 0
CUI: C1968790
Disease: Axonal degeneration/regeneration
Axonal degeneration/regeneration 		8 0 1 8.3E-02 0 0
CUI: C0235983
Disease: Normochromic anemia
Normochromic anemia 		9 0 1 7.7E-02 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw 		9 0 1 7.7E-02 0 0
CUI: C4025830
Disease: Peripheral axonal degeneration
Peripheral axonal degeneration 		9 0 1 7.7E-02 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 0 1 7.1E-02 0 0
CUI: C0340968
Disease: Deficiency of pyruvate kinase
Deficiency of pyruvate kinase 		10 0 1 7.1E-02 0 0
CUI: C0751576
Disease: Partial Paralysis (Paresis) Vocal Cords
Partial Paralysis (Paresis) Vocal Cords 		10 0 1 7.1E-02 0 0
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 3 7.0E-02 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation 		28 0 2 6.5E-02 0 0
CUI: C1858285
Disease: Decreased number of peripheral myelinated nerve fibers
Decreased number of peripheral myelinated nerve fibers 		28 0 2 6.5E-02 0 0
CUI: C0085577
Disease: Normocytic anemia
Normocytic anemia 		12 0 1 6.2E-02 0 0
CUI: C0015396
Disease: Eye Color
Eye Color 		13 0 1 5.9E-02 0 0
CUI: C4025735
Disease: Nonspherocytic hemolytic anemia
Nonspherocytic hemolytic anemia 		13 0 1 5.9E-02 0 0
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone 		14 0 1 5.6E-02 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		14 0 1 5.6E-02 0 0
CUI: C0520572
Disease: Enzymopathy
Enzymopathy 		17 0 1 4.8E-02 0 0
CUI: C1837496
Disease: Axonal degeneration
Axonal degeneration 		17 0 1 4.8E-02 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 4 4.6E-02 0 0
CUI: C0016506
Disease: Foot Deformities
Foot Deformities 		66 0 3 4.4E-02 0 0
CUI: C1879344
Disease: Biliary papillomatosis
Biliary papillomatosis 		20 0 1 4.2E-02 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 2 4.1E-02 0 0
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		21 0 1 4.0E-02 0 0
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		21 0 1 4.0E-02 0 0
CUI: C2875300
Disease: Peroneal muscular atrophy (axonal type) (hypertrophic type)
Peroneal muscular atrophy (axonal type) (hypertrophic type) 		21 0 1 4.0E-02 0 0