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: C0751576
Disease: Partial Paralysis (Paresis) Vocal Cords
Partial Paralysis (Paresis) Vocal Cords 		10 0 4 0.25 0 0
CUI: C1853710
Disease: HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)
HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder) 		5 0 3 0.25 0 0
CUI: C2079538
Disease: Charcot-Marie-Tooth disease, Type 2A
Charcot-Marie-Tooth disease, Type 2A 		7 0 3 0.21 0 0
CUI: C1847896
Disease: Charcot-Marie-Tooth Disease, Dominant Intermediate A
Charcot-Marie-Tooth Disease, Dominant Intermediate A 		2 0 2 0.20 0 0
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy 		14 0 4 0.20 0 0
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S 		9 0 3 0.19 0 0
CUI: C0240733
Disease: Peroneal muscle weakness
Peroneal muscle weakness 		3 0 2 0.18 0 0
CUI: C1837552
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder) 		3 0 2 0.18 0 0
CUI: C0264789
Disease: Familial cardiomyopathy
Familial cardiomyopathy 		10 0 3 0.18 0 0
CUI: C1851542
Disease: Limited hip movement
Limited hip movement 		10 0 3 0.18 0 0
CUI: C0750403
Disease: Proximal weakness
Proximal weakness 		11 0 3 0.17 0 0
CUI: C1850816
Disease: Decreased/absent ankle reflexes
Decreased/absent ankle reflexes 		4 0 2 0.17 0 0
CUI: C3148763
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E 		4 0 2 0.17 0 0
CUI: C3805969
Disease: Scapular muscle atrophy
Scapular muscle atrophy 		4 0 2 0.17 0 0
CUI: C3888087
Disease: Charcot-Marie-Tooth disease, Type 2I
Charcot-Marie-Tooth disease, Type 2I 		4 0 2 0.17 0 0
CUI: C4025619
Disease: Peripheral axonal atrophy
Peripheral axonal atrophy 		4 0 2 0.17 0 0
CUI: C0751036
Disease: Hereditary Motor and Sensory Neuropathy Type I
Hereditary Motor and Sensory Neuropathy Type I 		19 0 4 0.16 0 0
CUI: C1854150
Disease: Charcot-Marie-Tooth disease, Type 2B2
Charcot-Marie-Tooth disease, Type 2B2 		5 0 2 0.15 0 0
CUI: C4024612
Disease: Tibialis muscle weakness
Tibialis muscle weakness 		5 0 2 0.15 0 0
CUI: C4024613
Disease: Progressive distal muscular atrophy
Progressive distal muscular atrophy 		5 0 2 0.15 0 0
CUI: C1836057
Disease: Muscle fiber splitting
Muscle fiber splitting 		13 0 3 0.15 0 0
CUI: C1832931
Disease: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2 		6 0 2 0.14 0 0
CUI: C1847823
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F 		6 0 2 0.14 0 0
CUI: C1836767
Disease: Proximal lower limb amyotrophy
Proximal lower limb amyotrophy 		15 0 3 0.14 0 0
CUI: C4721916
Disease: HMSN Type V
HMSN Type V 		7 0 2 0.13 0 0