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: C4022646
Disease: Reduced muscle fiber alpha dystroglycan
Reduced muscle fiber alpha dystroglycan 		10 0 5 6.8E-02 0 0
CUI: C0521174
Disease: Microcalcification
Microcalcification 		42 0 7 6.8E-02 0 0
CUI: C1263858
Disease: Muscular dystrophy congenital, merosin negative
Muscular dystrophy congenital, merosin negative 		12 0 5 6.7E-02 0 0
CUI: C0263628
Disease: Tumoral calcinosis
Tumoral calcinosis 		45 0 7 6.6E-02 0 0
CUI: C2931687
Disease: Dysferlinopathy
Dysferlinopathy 		30 0 6 6.5E-02 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 8 6.5E-02 0 0
CUI: C0023485
Disease: Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma 		145 0 13 6.5E-02 0 0
CUI: C0410173
Disease: Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder) 		14 0 5 6.5E-02 0 0
CUI: C1836373
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K 		14 0 5 6.5E-02 0 0
CUI: C1847762
Disease: Cerebellar cyst
Cerebellar cyst 		14 0 5 6.5E-02 0 0
CUI: C4284790
Disease: Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1
Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 		14 16 5 6.5E-02 1 2.9E-02
CUI: C0231712
Disease: Waddling gait
Waddling gait 		113 0 11 6.5E-02 0 0
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		280 0 21 6.4E-02 0 0
CUI: C2936406
Disease: alpha-Dystroglycanopathies
alpha-Dystroglycanopathies 		15 0 5 6.4E-02 0 0
CUI: C4022916
Disease: Abnormal aldolase level
Abnormal aldolase level 		16 0 5 6.3E-02 0 0
CUI: C0546264
Disease: Congenital Fiber Type Disproportion
Congenital Fiber Type Disproportion 		33 0 6 6.3E-02 0 0
CUI: C0035313
Disease: Retinal Dysplasia
Retinal Dysplasia 		34 0 6 6.2E-02 0 0
CUI: C0877009
Disease: Muscle fibrosis
Muscle fibrosis 		34 0 6 6.2E-02 0 0
CUI: C1869123
Disease: Limb-girdle muscular dystrophy type 2A
Limb-girdle muscular dystrophy type 2A 		18 0 5 6.2E-02 0 0
CUI: C4025773
Disease: Aplasia/Hypoplasia involving the skeletal musculature
Aplasia/Hypoplasia involving the skeletal musculature 		19 0 5 6.1E-02 0 0
CUI: C4073168
Disease: Abnormal lactate dehydrogenase activity
Abnormal lactate dehydrogenase activity 		19 0 5 6.1E-02 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 7 6.1E-02 0 0
CUI: C1850830
Disease: Exercise-induced myalgia
Exercise-induced myalgia 		37 0 6 6.1E-02 0 0
CUI: C1527383
Disease: Morphea
Morphea 		20 0 5 6.0E-02 0 0
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia 		21 0 5 6.0E-02 0 0