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 1.2E-03 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		57 0 1 1.2E-03 0 0
CUI: C0518026
Disease: body fat percentage (physical finding)
body fat percentage (physical finding) 		56 0 1 1.2E-03 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		56 0 1 1.2E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 1 1.2E-03 0 0
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		55 0 1 1.2E-03 0 0
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		54 0 1 1.2E-03 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 1 1.2E-03 0 0
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		53 0 1 1.2E-03 0 0
CUI: C0345354
Disease: Radial polydactyly
Radial polydactyly 		51 0 1 1.2E-03 0 0
CUI: C0426789
Disease: Short thorax
Short thorax 		51 0 1 1.2E-03 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		50 116 1 1.2E-03 1 3.3E-03
CUI: C4317146
Disease: Acid reflux
Acid reflux 		50 0 1 1.2E-03 0 0
CUI: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1 		49 0 1 1.2E-03 0 0
CUI: C1836450
Disease: Distal lower limb muscle weakness
Distal lower limb muscle weakness 		49 0 1 1.2E-03 0 0
CUI: C1865037
Disease: Cone-shaped epiphysis
Cone-shaped epiphysis 		49 0 1 1.2E-03 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm 		48 0 1 1.2E-03 0 0
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		46 0 1 1.2E-03 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 1.3E-03 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 1.3E-03 0 0
CUI: C2673431
Disease: Abnormality of the periventricular white matter
Abnormality of the periventricular white matter 		45 0 1 1.3E-03 0 0
CUI: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1 		45 0 1 1.3E-03 0 0
CUI: C0015930
Disease: Fetal Distress
Fetal Distress 		44 0 1 1.3E-03 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis 		44 0 1 1.3E-03 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 1 1.3E-03 0 0