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: C1853932
Disease: Rimmed vacuoles on biopsy
Rimmed vacuoles on biopsy 		28 0 5 8.9E-02 0 0
CUI: C4728047
Disease: Left anterior descending coronary artery occlusion
Left anterior descending coronary artery occlusion 		5 0 3 8.6E-02 0 0
CUI: C0751951
Disease: Central Core Myopathy (disorder)
Central Core Myopathy (disorder) 		44 0 6 8.5E-02 0 0
CUI: C0270985
Disease: Alcohol myopathy
Alcohol myopathy 		6 0 3 8.3E-02 0 0
CUI: C1370868
Disease: Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive
Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive 		6 0 3 8.3E-02 0 0
CUI: C3888004
Disease: HERMANSKY-PUDLAK SYNDROME 5
HERMANSKY-PUDLAK SYNDROME 5 		6 0 3 8.3E-02 0 0
CUI: C0238190
Disease: Inclusion Body Myositis (disorder)
Inclusion Body Myositis (disorder) 		87 0 9 8.1E-02 0 0
CUI: C0018425
Disease: Gyrate Atrophy
Gyrate Atrophy 		8 0 3 7.9E-02 0 0
CUI: C1135188
Disease: Critical illness myopathy
Critical illness myopathy 		8 0 3 7.9E-02 0 0
CUI: C0476237
Disease: Metabolic symptoms
Metabolic symptoms 		9 0 3 7.7E-02 0 0
CUI: C0546483
Disease: Lung cyst
Lung cyst 		9 0 3 7.7E-02 0 0
CUI: C1737261
Disease: Acute myeloid leukaemia progression
Acute myeloid leukaemia progression 		9 0 3 7.7E-02 0 0
CUI: C2718001
Disease: Protein Misfolding Disorders
Protein Misfolding Disorders 		38 0 5 7.6E-02 0 0
CUI: C0751699
Disease: Minimally Conscious State
Minimally Conscious State 		12 0 3 7.1E-02 0 0
CUI: C0017097
Disease: Gardner Syndrome
Gardner Syndrome 		29 0 4 6.9E-02 0 0
CUI: C0398368
Disease: Lymphatic Abnormalities
Lymphatic Abnormalities 		30 0 4 6.8E-02 0 0
CUI: C0155686
Disease: Acute myocarditis
Acute myocarditis 		33 0 4 6.5E-02 0 0
CUI: C4021082
Disease: Fatty replacement of skeletal muscle
Fatty replacement of skeletal muscle 		17 0 3 6.4E-02 0 0
CUI: C0029401
Disease: Osteitis Deformans
Osteitis Deformans 		134 0 10 6.4E-02 0 0
CUI: C0877009
Disease: Muscle fibrosis
Muscle fibrosis 		34 0 4 6.3E-02 0 0
CUI: C1833662
Disease: INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA 		34 0 4 6.3E-02 0 0
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		18 0 3 6.2E-02 0 0
CUI: C0740985
Disease: Acute anaemia
Acute anaemia 		18 0 3 6.2E-02 0 0
CUI: C1279412
Disease: periodic paralysis (finding)
periodic paralysis (finding) 		18 0 3 6.2E-02 0 0
CUI: C1257763
Disease: Overnutrition
Overnutrition 		54 0 5 6.1E-02 0 0