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: C0520888
Disease: Inverted T wave
Inverted T wave 		4 0 3 0.33 0 0
CUI: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		7 0 2 0.15 0 0
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		7 0 2 0.15 0 0
CUI: C2748884
Disease: CARDIOMYOPATHY, INFANTILE HYPERTROPHIC
CARDIOMYOPATHY, INFANTILE HYPERTROPHIC 		9 0 2 0.13 0 0
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		9 0 2 0.13 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 0 2 0.12 0 0
CUI: C0392178
Disease: Lipiduria
Lipiduria 		1 0 1 0.12 0 0
CUI: C1706559
Disease: Cornea verticillata
Cornea verticillata 		1 0 1 0.12 0 0
CUI: C1834460
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10 		1 0 1 0.12 0 0
CUI: C1837471
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8 		1 8 1 0.12 1 1.0E-01
CUI: C1856697
Disease: Mitochondrial malic enzyme reduced
Mitochondrial malic enzyme reduced 		1 0 1 0.12 0 0
CUI: C2751427
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO 		1 0 1 0.12 0 0
CUI: C2751807
Disease: Emery-Dreifuss Muscular Dystrophy 4
Emery-Dreifuss Muscular Dystrophy 4 		1 0 1 0.12 0 0
CUI: C3150754
Disease: GLYCOGEN STORAGE DISEASE XV
GLYCOGEN STORAGE DISEASE XV 		1 0 1 0.12 0 0
CUI: C3665332
Disease: Primary hypertrophic cardiomyopathy
Primary hypertrophic cardiomyopathy 		1 0 1 0.12 0 0
CUI: C3683483
Disease: Autosomal Recessive Cerebellar Ataxia Type 1
Autosomal Recessive Cerebellar Ataxia Type 1 		1 0 1 0.12 0 0
CUI: C3715165
Disease: LEFT VENTRICULAR NONCOMPACTION 10
LEFT VENTRICULAR NONCOMPACTION 10 		1 0 1 0.12 0 0
CUI: C3809346
Disease: CARDIOMYOPATHY, DILATED, 1MM
CARDIOMYOPATHY, DILATED, 1MM 		1 0 1 0.12 0 0
CUI: C4015452
Disease: POLYGLUCOSAN BODY MYOPATHY 2
POLYGLUCOSAN BODY MYOPATHY 2 		1 0 1 0.12 0 0
CUI: C4021047
Disease: Impaired visually enhanced vestibulo-ocular reflex
Impaired visually enhanced vestibulo-ocular reflex 		1 0 1 0.12 0 0
CUI: C4024899
Disease: Atrophy/Degeneration affecting the central nervous system
Atrophy/Degeneration affecting the central nervous system 		1 0 1 0.12 0 0
CUI: C4025641
Disease: Decreased pyruvate carboxylase activity
Decreased pyruvate carboxylase activity 		1 0 1 0.12 0 0
CUI: C4707155
Disease: Autosomal recessive myogenic arthrogryposis multiplex congenita
Autosomal recessive myogenic arthrogryposis multiplex congenita 		1 0 1 0.12 0 0
CUI: C4732796
Disease: Apical hypertrophic cardiomyopathy
Apical hypertrophic cardiomyopathy 		10 0 2 0.12 0 0
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 0 3 0.12 0 0