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: C0016512
Disease: Foot pain
Foot pain 		1 0 1 2.0E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 2.0E-02 0 0
CUI: C0267548
Disease: Ileocolic intussusception
Ileocolic intussusception 		1 0 1 2.0E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 2.0E-02 0 0
CUI: C0454643
Disease: Word finding difficulty (disorder)
Word finding difficulty (disorder) 		1 0 1 2.0E-02 0 0
CUI: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria 		1 0 1 2.0E-02 0 0
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia 		1 0 1 2.0E-02 0 0
CUI: C0558384
Disease: Arthritis/arthrosis
Arthritis/arthrosis 		1 0 1 2.0E-02 0 0
CUI: C0576690
Disease: Impaired body position sense
Impaired body position sense 		1 0 1 2.0E-02 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 2.0E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 2.0E-02 0 0
CUI: C1833202
Disease: LCHAD DEFICIENCY WITH MATERNAL ACUTE FATTY LIVER OF PREGNANCY
LCHAD DEFICIENCY WITH MATERNAL ACUTE FATTY LIVER OF PREGNANCY 		1 0 1 2.0E-02 0 0
CUI: C1834692
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA 		1 0 1 2.0E-02 0 0
CUI: C1835093
Disease: Masticatory Muscles, Hypertrophy of
Masticatory Muscles, Hypertrophy of 		1 0 1 2.0E-02 0 0
CUI: C1836050
Disease: Filaminopathy, autosomal dominant
Filaminopathy, autosomal dominant 		1 0 1 2.0E-02 0 0
CUI: C1836439
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 		1 0 1 2.0E-02 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 0 1 2.0E-02 0 0
CUI: C1836448
Disease: Nemaline myopathy 1
Nemaline myopathy 1 		1 0 1 2.0E-02 0 0
CUI: C1836460
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 		1 0 1 2.0E-02 0 0
CUI: C1836472
Disease: Nemaline myopathy 6
Nemaline myopathy 6 		1 0 1 2.0E-02 0 0
CUI: C1836485
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder) 		1 0 1 2.0E-02 0 0
CUI: C1839028
Disease: Mitochondrial Myopathy with Diabetes
Mitochondrial Myopathy with Diabetes 		1 0 1 2.0E-02 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 2.0E-02 0 0
CUI: C1842898
Disease: Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency 		1 0 1 2.0E-02 0 0
CUI: C1843791
Disease: CARDIOMYOPATHY, DILATED, 1N
CARDIOMYOPATHY, DILATED, 1N 		1 0 1 2.0E-02 0 0