Source: CURATED ×
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: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		8 5 8 1.00 5 9.8E-02
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		8 0 8 1.00 0 0
CUI: C0751036
Disease: Hereditary Motor and Sensory Neuropathy Type I
Hereditary Motor and Sensory Neuropathy Type I 		8 84 8 1.00 28 0.26
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		12 52 8 0.67 3 3.0E-02
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		13 0 8 0.62 0 0
CUI: C0019816
Disease: Hereditary, Type VII, Motor and Sensory Neuropathy
Hereditary, Type VII, Motor and Sensory Neuropathy 		6 0 2 0.17 0 0
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		6 0 2 0.17 0 0
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder) 		7 28 2 0.15 9 0.13
CUI: C0009676
Disease: Confusion
Confusion 		1 0 1 0.12 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot 		1 0 1 0.12 0 0
CUI: C0018378
Disease: Guillain-Barre Syndrome
Guillain-Barre Syndrome 		1 0 1 0.12 0 0
CUI: C0152237
Disease: Talipes Calcaneovalgus
Talipes Calcaneovalgus 		1 0 1 0.12 0 0
CUI: C0233715
Disease: Speech impairment
Speech impairment 		1 0 1 0.12 0 0
CUI: C0233754
Disease: Derealization
Derealization 		1 0 1 0.12 0 0
CUI: C0240912
Disease: Vertical Talus
Vertical Talus 		1 0 1 0.12 0 0
CUI: C0265280
Disease: Spondylometaphyseal dysplasia, Kozlowski type
Spondylometaphyseal dysplasia, Kozlowski type 		1 0 1 0.12 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism 		1 0 1 0.12 0 0
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		1 0 1 0.12 0 0
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3 		1 0 1 0.12 0 0
CUI: C0562557
Disease: Sexually disinhibited behavior
Sexually disinhibited behavior 		1 0 1 0.12 0 0
CUI: C0751226
Disease: Hypersomnia, Recurrent
Hypersomnia, Recurrent 		1 0 1 0.12 0 0
CUI: C1837805
Disease: Charcot-Marie-Tooth disease, axonal, Type 2G
Charcot-Marie-Tooth disease, axonal, Type 2G 		1 0 1 0.12 0 0
CUI: C1838492
Disease: SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder)
SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder) 		1 0 1 0.12 0 0
CUI: C1843075
Disease: Charcot-Marie-Tooth Disease, Dominant Intermediate D
Charcot-Marie-Tooth Disease, Dominant Intermediate D 		1 6 1 0.12 6 0.12
CUI: C1843153
Disease: Charcot-Marie-Tooth disease, Type 2J
Charcot-Marie-Tooth disease, Type 2J 		1 7 1 0.12 5 9.4E-02