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: C0005910
Disease: Body Weight
Body Weight 		57 0 1 1.9E-03 0 0
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		57 0 1 1.9E-03 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor 		57 0 1 1.9E-03 0 0
CUI: C0751882
Disease: Myasthenic Syndromes, Congenital
Myasthenic Syndromes, Congenital 		57 0 1 1.9E-03 0 0
CUI: C1862863
Disease: Sparse body hair
Sparse body hair 		57 0 1 1.9E-03 0 0
CUI: C0015393
Disease: Eye Abnormalities
Eye Abnormalities 		55 0 1 1.9E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 1 1.9E-03 0 0
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		55 0 1 1.9E-03 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential 		55 0 1 1.9E-03 0 0
CUI: C1858025
Disease: Spinal rigidity
Spinal rigidity 		55 0 1 1.9E-03 0 0
CUI: C4020847
Disease: Abnormality of pelvic girdle bone morphology
Abnormality of pelvic girdle bone morphology 		55 0 1 1.9E-03 0 0
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		54 0 1 1.9E-03 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 1 1.9E-03 0 0
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		54 0 1 1.9E-03 0 0
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		54 0 1 1.9E-03 0 0
CUI: C0017979
Disease: Glycosuria
Glycosuria 		53 0 1 1.9E-03 0 0
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		53 0 1 1.9E-03 0 0
CUI: C1860816
Disease: Preauricular skin tag
Preauricular skin tag 		53 0 1 1.9E-03 0 0
CUI: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges 		52 0 1 1.9E-03 0 0
CUI: C0085576
Disease: Iron-Refractory Iron Deficiency Anemia
Iron-Refractory Iron Deficiency Anemia 		51 0 1 1.9E-03 0 0
CUI: C0342751
Disease: Generalized glycogen storage disease of infants
Generalized glycogen storage disease of infants 		51 0 1 1.9E-03 0 0
CUI: C0342776
Disease: Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency 		51 0 1 1.9E-03 0 0
CUI: C0345354
Disease: Radial polydactyly
Radial polydactyly 		51 0 1 1.9E-03 0 0
CUI: C0426789
Disease: Short thorax
Short thorax 		51 0 1 1.9E-03 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		51 0 1 1.9E-03 0 0