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: C1852502
Disease: CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT 		45 9 44 0.64 3 0.12
CUI: C2827469
Disease: Coronary Microvascular Disease
Coronary Microvascular Disease 		45 3 44 0.64 3 0.15
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		54 20 15 0.14 1 2.6E-02
CUI: C2936331
Disease: Sarcoglycanopathies
Sarcoglycanopathies 		20 0 10 0.13 0 0
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		46 0 12 0.12 0 0
CUI: C0410174
Disease: Fukuyama Type Congenital Muscular Dystrophy
Fukuyama Type Congenital Muscular Dystrophy 		35 0 9 9.6E-02 0 0
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness 		41 0 9 9.0E-02 0 0
CUI: C1834674
Disease: BETHLEM MYOPATHY 1
BETHLEM MYOPATHY 1 		17 0 7 9.0E-02 0 0
CUI: C1839666
Disease: Calf muscle pseudohypertrophy
Calf muscle pseudohypertrophy 		17 0 7 9.0E-02 0 0
CUI: C2875316
Disease: Myotubular (centronuclear) myopathy
Myotubular (centronuclear) myopathy 		10 0 6 8.3E-02 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 9 8.2E-02 0 0
CUI: C0024003
Disease: Lordosis
Lordosis 		160 0 17 8.1E-02 0 0
CUI: C1850794
Disease: Proximal amyotrophy
Proximal amyotrophy 		29 0 7 7.8E-02 0 0
CUI: C0270962
Disease: Multi-core congenital myopathy
Multi-core congenital myopathy 		16 0 6 7.7E-02 0 0
CUI: C0457133
Disease: Muscle eye brain disease
Muscle eye brain disease 		19 0 6 7.4E-02 0 0
CUI: C1879312
Disease: Agyria
Agyria 		20 0 6 7.3E-02 0 0
CUI: C0427144
Disease: Toe-walking gait
Toe-walking gait 		50 0 8 7.3E-02 0 0
CUI: C0265221
Disease: Walker-Warburg congenital muscular dystrophy
Walker-Warburg congenital muscular dystrophy 		21 0 6 7.2E-02 0 0
CUI: C0006663
Disease: Calcinosis
Calcinosis 		52 0 8 7.1E-02 0 0
CUI: C0431376
Disease: Cobblestone Lissencephaly
Cobblestone Lissencephaly 		23 0 6 7.1E-02 0 0
CUI: C1842552
Disease: Limb-girdle muscle atrophy
Limb-girdle muscle atrophy 		8 0 5 7.0E-02 0 0
CUI: C1858025
Disease: Spinal rigidity
Spinal rigidity 		55 0 8 7.0E-02 0 0
CUI: C0917713
Disease: Becker Muscular Dystrophy
Becker Muscular Dystrophy 		86 0 10 6.9E-02 0 0
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle 		118 37 12 6.9E-02 1 1.8E-02
CUI: C4015098
Disease: Hypoglycosylation of alpha-dystroglycan
Hypoglycosylation of alpha-dystroglycan 		10 0 5 6.8E-02 0 0