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: C0393626
Disease: Opsoclonus-Myoclonus Syndrome
Opsoclonus-Myoclonus Syndrome 		14 0 1 6.7E-02 0 0
CUI: C0085543
Disease: Epilepsia Partialis Continua
Epilepsia Partialis Continua 		15 0 1 6.2E-02 0 0
CUI: C0684219
Disease: Myokymia
Myokymia 		15 0 1 6.2E-02 0 0
CUI: C4477055
Disease: Limb myoclonus
Limb myoclonus 		15 0 1 6.2E-02 0 0
CUI: C1855580
Disease: Exercise-induced muscle fatigue
Exercise-induced muscle fatigue 		18 3 1 5.3E-02 1 0.20
CUI: C0231274
Disease: Intolerant of heat
Intolerant of heat 		19 7 1 5.0E-02 1 0.11
CUI: C0751036
Disease: Hereditary Motor and Sensory Neuropathy Type I
Hereditary Motor and Sensory Neuropathy Type I 		19 0 1 5.0E-02 0 0
CUI: C0034880
Disease: Hyperacusis
Hyperacusis 		20 9 1 4.8E-02 1 9.1E-02
CUI: C1857539
Disease: Deep palmar crease
Deep palmar crease 		23 8 1 4.2E-02 2 0.22
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		26 0 1 3.7E-02 0 0
CUI: C0239842
Disease: Tremor of hands
Tremor of hands 		31 7 1 3.1E-02 1 0.11
CUI: C4022748
Disease: Focal T2 hyperintense brainstem lesion
Focal T2 hyperintense brainstem lesion 		33 2 1 2.9E-02 1 0.25
CUI: C0241703
Disease: High pitched voice
High pitched voice 		35 0 1 2.8E-02 0 0
CUI: C0542223
Disease: Loss of speech
Loss of speech 		37 8 1 2.6E-02 2 0.22
CUI: C1849097
Disease: Loss of ability to walk
Loss of ability to walk 		37 11 1 2.6E-02 2 0.17
CUI: C4023342
Disease: Gastrostomy tube feeding in infancy
Gastrostomy tube feeding in infancy 		38 19 1 2.6E-02 2 1.0E-01
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		42 0 1 2.3E-02 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 3 1 2.1E-02 1 0.20
CUI: C0401149
Disease: Chronic constipation
Chronic constipation 		47 16 1 2.1E-02 1 5.6E-02
CUI: C0920299
Disease: Overriding toe
Overriding toe 		47 13 1 2.1E-02 1 6.7E-02
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 0 1 2.0E-02 0 0
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive 		48 0 1 2.0E-02 0 0
CUI: C1867131
Disease: Broad hallux
Broad hallux 		48 14 1 2.0E-02 1 6.2E-02
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses 		51 0 1 1.9E-02 0 0
CUI: C0751785
Disease: Unverricht-Lundborg Syndrome
Unverricht-Lundborg Syndrome 		56 0 1 1.8E-02 0 0