Source: CLINVAR ×
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: C0241237
Disease: Difficulty standing
Difficulty standing 		8 0 4 0.25 0 0
CUI: C1836767
Disease: Proximal lower limb amyotrophy
Proximal lower limb amyotrophy 		3 0 3 0.25 0 0
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		4 0 3 0.23 0 0
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness 		4 4 3 0.23 1 5.9E-02
CUI: C0558845
Disease: Reflex, Ankle, Absent
Reflex, Ankle, Absent 		4 5 3 0.23 1 5.6E-02
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		21 48 6 0.22 2 3.3E-02
CUI: C0027868
Disease: Neuromuscular Diseases
Neuromuscular Diseases 		11 0 4 0.21 0 0
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle 		7 0 3 0.19 0 0
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		8 0 3 0.18 0 0
CUI: C4021765
Disease: Morphological abnormality of the central nervous system
Morphological abnormality of the central nervous system 		8 0 3 0.18 0 0
CUI: C0004239
Disease: Atrial Flutter
Atrial Flutter 		2 0 2 0.17 0 0
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		2 0 2 0.17 0 0
CUI: C0340477
Disease: Re-entrant atrioventricular tachycardia
Re-entrant atrioventricular tachycardia 		2 0 2 0.17 0 0
CUI: C0428974
Disease: Supraventricular arrhythmia
Supraventricular arrhythmia 		2 0 2 0.17 0 0
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S 		9 0 3 0.17 0 0
CUI: C1836118
Disease: LEFT VENTRICULAR NONCOMPACTION 2
LEFT VENTRICULAR NONCOMPACTION 2 		2 0 2 0.17 0 0
CUI: C1837342
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J 		2 0 2 0.17 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		2 0 2 0.17 0 0
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g 		2 0 2 0.17 0 0
CUI: C1861065
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9 		2 0 2 0.17 0 0
CUI: C1863599
Disease: Hereditary Myopathy with Early Respiratory Failure
Hereditary Myopathy with Early Respiratory Failure 		2 0 2 0.17 0 0
CUI: C2673677
Disease: Myopathy, Early-Onset, with Fatal Cardiomyopathy
Myopathy, Early-Onset, with Fatal Cardiomyopathy 		2 0 2 0.17 0 0
CUI: C3277184
Disease: Decreased patellar reflex
Decreased patellar reflex 		2 0 2 0.17 0 0
CUI: C3805969
Disease: Scapular muscle atrophy
Scapular muscle atrophy 		2 0 2 0.17 0 0
CUI: C4021054
Disease: Reduced muscle collagen VI
Reduced muscle collagen VI 		2 0 2 0.17 0 0