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: C0268123
Disease: Muscle AMP deaminase deficiency
Muscle AMP deaminase deficiency 		4 0 3 0.30 0 0
CUI: C0151236
Disease: Conduction system abnormalities
Conduction system abnormalities 		3 0 2 0.20 0 0
CUI: C0340420
Disease: Cardiac glycogenosis
Cardiac glycogenosis 		3 0 2 0.20 0 0
CUI: C3899154
Disease: familial testicular germ cell tumor
familial testicular germ cell tumor 		4 0 2 0.18 0 0
CUI: C1442981
Disease: Alcoholic liver damage
Alcoholic liver damage 		6 0 2 0.15 0 0
CUI: C0017924
Disease: Glycogen Storage Disease Type V
Glycogen Storage Disease Type V 		22 0 4 0.15 0 0
CUI: C0268104
Disease: Disorder of purine metabolism
Disorder of purine metabolism 		7 0 2 0.14 0 0
CUI: C1291390
Disease: Deficiency of phosphorylase kinase
Deficiency of phosphorylase kinase 		8 0 2 0.13 0 0
CUI: C1855578
Disease: Exercise-induced muscle cramps
Exercise-induced muscle cramps 		8 0 2 0.13 0 0
CUI: C0151773
Disease: Bone marrow depression
Bone marrow depression 		9 0 2 0.12 0 0
CUI: C0270984
Disease: Metabolic myopathy
Metabolic myopathy 		18 0 3 0.12 0 0
CUI: C1689817
Disease: Cardiomyopathy associated with another disorder
Cardiomyopathy associated with another disorder 		10 0 2 0.12 0 0
CUI: C0011859
Disease: Lipoatrophic Diabetes Mellitus
Lipoatrophic Diabetes Mellitus 		11 0 2 0.11 0 0
CUI: C0268121
Disease: APRT deficiency, Japanese type
APRT deficiency, Japanese type 		1 0 1 0.11 0 0
CUI: C0878677
Disease: Glycogen Storage Disease Type IIb
Glycogen Storage Disease Type IIb 		11 0 2 0.11 0 0
CUI: C1865290
Disease: Hyperinsulinemic hypoglycemia, familial, 3
Hyperinsulinemic hypoglycemia, familial, 3 		1 0 1 0.11 0 0
CUI: C1960396
Disease: Epidermal growth factor receptor negative non-small cell lung cancer
Epidermal growth factor receptor negative non-small cell lung cancer 		1 0 1 0.11 0 0
CUI: C2609269
Disease: Fasting hyperglycaemia
Fasting hyperglycaemia 		1 0 1 0.11 0 0
CUI: C2752073
Disease: Erythrocyte Amp Deaminase Deficiency
Erythrocyte Amp Deaminase Deficiency 		1 0 1 0.11 0 0
CUI: C4016117
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET
DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET 		1 0 1 0.11 0 0
CUI: C4017156
Disease: MCARDLE DISEASE, MILD
MCARDLE DISEASE, MILD 		1 0 1 0.11 0 0
CUI: C4310619
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59 		1 0 1 0.11 0 0
CUI: C0025637
Disease: Methemoglobinemia
Methemoglobinemia 		12 0 2 0.11 0 0
CUI: C0751007
Disease: Intracranial Atherosclerosis
Intracranial Atherosclerosis 		12 0 2 0.11 0 0
CUI: C0010074
Disease: Coronary Vessel Anomalies
Coronary Vessel Anomalies 		2 0 1 1.0E-01 0 0