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: C0015464
Disease: Facial Nerve Diseases
Facial Nerve Diseases 		1 0 1 6.2E-02 0 0
CUI: C0267548
Disease: Ileocolic intussusception
Ileocolic intussusception 		1 0 1 6.2E-02 0 0
CUI: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure 		1 0 1 6.2E-02 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 6.2E-02 0 0
CUI: C0558384
Disease: Arthritis/arthrosis
Arthritis/arthrosis 		1 0 1 6.2E-02 0 0
CUI: C1332312
Disease: Aortic Angiosarcoma
Aortic Angiosarcoma 		1 0 1 6.2E-02 0 0
CUI: C1655035
Disease: congenital muscle disorder
congenital muscle disorder 		1 0 1 6.2E-02 0 0
CUI: C1835093
Disease: Masticatory Muscles, Hypertrophy of
Masticatory Muscles, Hypertrophy of 		1 0 1 6.2E-02 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 0 1 6.2E-02 0 0
CUI: C1836448
Disease: Nemaline myopathy 1
Nemaline myopathy 1 		1 0 1 6.2E-02 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 6.2E-02 0 0
CUI: C1847902
Disease: CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder)
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder) 		1 0 1 6.2E-02 0 0
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 0 1 6.2E-02 0 0
CUI: C1861753
Disease: Multiminicore Disease, Moderate, with Hand Involvement
Multiminicore Disease, Moderate, with Hand Involvement 		1 0 1 6.2E-02 0 0
CUI: C2083352
Disease: Rectus femoris muscle atrophy
Rectus femoris muscle atrophy 		1 0 1 6.2E-02 0 0
CUI: C2674259
Disease: NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder)
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder) 		1 0 1 6.2E-02 0 0
CUI: C2750413
Disease: Cap Myopathy, Tpm2-Related
Cap Myopathy, Tpm2-Related 		1 0 1 6.2E-02 0 0
CUI: C2750414
Disease: CAP MYOPATHY, TPM3-RELATED (disorder)
CAP MYOPATHY, TPM3-RELATED (disorder) 		1 0 1 6.2E-02 0 0
CUI: C2750536
Disease: Nemaline Myopathy 3, With Intranuclear Rods
Nemaline Myopathy 3, With Intranuclear Rods 		1 0 1 6.2E-02 0 0
CUI: C2750537
Disease: Myopathy, Actin, Congenital, With Cores
Myopathy, Actin, Congenital, With Cores 		1 0 1 6.2E-02 0 0
CUI: C2930980
Disease: Malignant hyperthermia susceptibility type 1
Malignant hyperthermia susceptibility type 1 		1 0 1 6.2E-02 0 0
CUI: C2936171
Disease: Familial Ebstein's Anomaly
Familial Ebstein's Anomaly 		1 0 1 6.2E-02 0 0
CUI: C3150690
Disease: LEFT VENTRICULAR NONCOMPACTION 5
LEFT VENTRICULAR NONCOMPACTION 5 		1 0 1 6.2E-02 0 0
CUI: C3553709
Disease: MYOPATHY, CENTRONUCLEAR, 4
MYOPATHY, CENTRONUCLEAR, 4 		1 0 1 6.2E-02 0 0
CUI: C3714994
Disease: CAP MYOPATHY 1
CAP MYOPATHY 1 		1 0 1 6.2E-02 0 0