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: C1968739
Disease: Glycogen Storage Disease IIIA
Glycogen Storage Disease IIIA 		1 0 1 0.50 0 0
CUI: C1968740
Disease: Glycogen Storage Disease IIIB
Glycogen Storage Disease IIIB 		1 0 1 0.50 0 0
CUI: C2936915
Disease: Amylo-1,6-glucosidase deficiency
Amylo-1,6-glucosidase deficiency 		1 0 1 0.50 0 0
CUI: C3695006
Disease: GLYCOGEN STORAGE DISEASE, TYPE IIIb
GLYCOGEN STORAGE DISEASE, TYPE IIIb 		1 0 1 0.50 0 0
CUI: C3695007
Disease: GLYCOGEN STORAGE DISEASE, TYPE IIIa
GLYCOGEN STORAGE DISEASE, TYPE IIIa 		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: C0751172
Disease: Adult Glycogen Storage Disease Type II
Adult Glycogen Storage Disease Type II 		2 0 1 0.33 0 0
CUI: C0751174
Disease: Glycogen Storage Disease Type II, Juvenile
Glycogen Storage Disease Type II, Juvenile 		2 0 1 0.33 0 0
CUI: C1850656
Disease: Firm muscles
Firm muscles 		2 0 1 0.33 0 0
CUI: C0751173
Disease: Glycogen Storage Disease Type II, Infantile
Glycogen Storage Disease Type II, Infantile 		4 0 1 0.20 0 0
CUI: C0520878
Disease: Shortened PR interval
Shortened PR interval 		6 0 1 0.14 0 0
CUI: C0220989
Disease: Acquired partial lipodystrophy
Acquired partial lipodystrophy 		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: C0017922
Disease: Glycogen Storage Disease Type III
Glycogen Storage Disease Type III 		8 125 1 0.11 1 8.0E-03
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: 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: C0035232
Disease: Respiratory Paralysis
Respiratory Paralysis 		13 0 1 7.1E-02 0 0
CUI: C0369183
Disease: Erythrocyte Mean Corpuscular Hemoglobin Test
Erythrocyte Mean Corpuscular Hemoglobin Test 		13 0 1 7.1E-02 0 0
CUI: C1704378
Disease: Heymann Nephritis
Heymann Nephritis 		13 0 1 7.1E-02 0 0
CUI: C4316789
Disease: Partial lipodystrophy
Partial lipodystrophy 		14 0 1 6.7E-02 0 0
CUI: C0270984
Disease: Metabolic myopathy
Metabolic myopathy 		18 0 1 5.3E-02 0 0
CUI: C1969443
Disease: Trifunctional Protein Deficiency With Myopathy And Neuropathy
Trifunctional Protein Deficiency With Myopathy And Neuropathy 		23 0 1 4.2E-02 0 0