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: C0751174
Disease: Glycogen Storage Disease Type II, Juvenile
Glycogen Storage Disease Type II, Juvenile 		2 0 2 1.00 0 0
CUI: C0751173
Disease: Glycogen Storage Disease Type II, Infantile
Glycogen Storage Disease Type II, Infantile 		4 0 2 0.50 0 0
CUI: C1832243
Disease: CARDIOMYOPATHY, DILATED, 1D (disorder)
CARDIOMYOPATHY, DILATED, 1D (disorder) 		1 0 1 0.50 0 0
CUI: C1861864
Disease: Cardiomyopathy, Familial Hypertrophic, 2
Cardiomyopathy, Familial Hypertrophic, 2 		1 0 1 0.50 0 0
CUI: C2676271
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder) 		1 0 1 0.50 0 0
CUI: C3888925
Disease: Pompe's disease adult onset
Pompe's disease adult onset 		1 0 1 0.50 0 0
CUI: C4016981
Disease: GLYCOGEN STORAGE DISEASE II, ADULT FORM
GLYCOGEN STORAGE DISEASE II, ADULT FORM 		1 0 1 0.50 0 0
CUI: C1841658
Disease: Progressive Familial Heart Block, Type II
Progressive Familial Heart Block, Type II 		2 0 1 0.33 0 0
CUI: C1850656
Disease: Firm muscles
Firm muscles 		2 0 1 0.33 0 0
CUI: C1968741
Disease: Glycogen Storage Disease IIIC
Glycogen Storage Disease IIIC 		2 0 1 0.33 0 0
CUI: C0348616
Disease: Other restrictive cardiomyopathy
Other restrictive cardiomyopathy 		5 0 1 0.17 0 0
CUI: C0520878
Disease: Shortened PR interval
Shortened PR interval 		6 0 1 0.14 0 0
CUI: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		7 0 1 0.12 0 0
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		7 0 1 0.12 0 0
CUI: C3888924
Disease: Glycogen storage disease due to acid maltase deficiency, infantile onset
Glycogen storage disease due to acid maltase deficiency, infantile onset 		7 0 1 0.12 0 0
CUI: C0342753
Disease: Glycogen storage disease due to acid maltase deficiency, late-onset
Glycogen storage disease due to acid maltase deficiency, late-onset 		8 0 1 0.11 0 0
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		9 0 1 1.0E-01 0 0
CUI: C4021152
Disease: Abnormal CNS myelination
Abnormal CNS myelination 		9 0 1 1.0E-01 0 0
CUI: C0017923
Disease: Glycogen Storage Disease Type IV
Glycogen Storage Disease Type IV 		10 0 1 9.1E-02 0 0
CUI: C0242973
Disease: Ventricular Dysfunction
Ventricular Dysfunction 		11 0 1 8.3E-02 0 0
CUI: C0523953
Disease: Cardiac troponin T measurement
Cardiac troponin T measurement 		11 0 1 8.3E-02 0 0
CUI: C0035232
Disease: Respiratory Paralysis
Respiratory Paralysis 		13 0 1 7.1E-02 0 0
CUI: C1704378
Disease: Heymann Nephritis
Heymann Nephritis 		13 0 1 7.1E-02 0 0
CUI: C0270984
Disease: Metabolic myopathy
Metabolic myopathy 		18 0 1 5.3E-02 0 0
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 0 1 4.5E-02 0 0