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: C4021055
Disease: Absent muscle fiber merosin
Absent muscle fiber merosin 		1 0 1 1.00 0 0
CUI: C4748327
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23
MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23 		1 12 1 1.00 1 5.6E-02
CUI: C0240017
Disease: Intercostal muscle weakness
Intercostal muscle weakness 		2 0 1 0.50 0 0
CUI: C4020790
Disease: Medullary sponge kidney disease
Medullary sponge kidney disease 		2 0 1 0.50 0 0
CUI: C0086588
Disease: Marasmus
Marasmus 		3 0 1 0.33 0 0
CUI: C0429494
Disease: Ocular axial length
Ocular axial length 		4 0 1 0.25 0 0
CUI: C1865318
Disease: Abnormality of the temporomandibular joint
Abnormality of the temporomandibular joint 		4 0 1 0.25 0 0
CUI: C4022749
Disease: Abnormal brainstem MRI signal intensity
Abnormal brainstem MRI signal intensity 		5 0 1 0.20 0 0
CUI: C1853766
Disease: Pontocerebellar atrophy
Pontocerebellar atrophy 		6 0 1 0.17 0 0
CUI: C4020908
Disease: Hypointensity of cerebral white matter on MRI
Hypointensity of cerebral white matter on MRI 		6 0 1 0.17 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 1 0.14 0 0
CUI: C4551860
Disease: Ullrich congenital muscular dystrophy
Ullrich congenital muscular dystrophy 		7 0 1 0.14 0 0
CUI: C4024942
Disease: Late-onset muscular dystrophy
Late-onset muscular dystrophy 		8 0 1 0.12 0 0
CUI: C0022681
Disease: Medullary sponge kidney
Medullary sponge kidney 		9 0 1 0.11 0 0
CUI: C0392553
Disease: Hereditary peripheral neuropathy
Hereditary peripheral neuropathy 		9 0 1 0.11 0 0
CUI: C4022161
Disease: Increased endomysial connective tissue
Increased endomysial connective tissue 		10 0 1 1.0E-01 0 0
CUI: C0343239
Disease: Benign congenital hypotonia
Benign congenital hypotonia 		11 0 1 9.1E-02 0 0
CUI: C1263858
Disease: Muscular dystrophy congenital, merosin negative
Muscular dystrophy congenital, merosin negative 		12 109 1 8.3E-02 4 3.6E-02
CUI: C0220787
Disease: Endotracheal aspiration
Endotracheal aspiration 		13 0 1 7.7E-02 0 0
CUI: C0700198
Disease: Pulmonary aspiration
Pulmonary aspiration 		13 0 1 7.7E-02 0 0
CUI: C1963221
Disease: Aspiration, CTCAE
Aspiration, CTCAE 		13 0 1 7.7E-02 0 0
CUI: C2827071
Disease: Unintentional Material Aspiration
Unintentional Material Aspiration 		13 0 1 7.7E-02 0 0
CUI: C0239043
Disease: Difficulty chewing
Difficulty chewing 		14 0 1 7.1E-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 1 7.1E-02 0 0
CUI: C1866021
Disease: Increased connective tissue
Increased connective tissue 		16 0 1 6.2E-02 0 0