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: C1866008
Disease: Muscular Dystrophy, Limb-Girdle, Type 2G
Muscular Dystrophy, Limb-Girdle, Type 2G 		1 0 1 3.3E-02 0 0
CUI: C1876166
Disease: Endemic Tyrolean Infantile Cirrhosis
Endemic Tyrolean Infantile Cirrhosis 		1 0 1 3.3E-02 0 0
CUI: C1969785
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder) 		1 0 1 3.3E-02 0 0
CUI: C2053440
Disease: Thin lower lip vermilion
Thin lower lip vermilion 		1 0 1 3.3E-02 0 0
CUI: C2083352
Disease: Rectus femoris muscle atrophy
Rectus femoris muscle atrophy 		1 0 1 3.3E-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 3.3E-02 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve 		1 0 1 3.3E-02 0 0
CUI: C2678015
Disease: Myopathy, Reducing Body, X-Linked, Childhood-Onset
Myopathy, Reducing Body, X-Linked, Childhood-Onset 		1 0 1 3.3E-02 0 0
CUI: C2678027
Disease: Myopathy, Reducing Body, X-Linked, Early-Onset, Severe
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe 		1 0 1 3.3E-02 0 0
CUI: C2678055
Disease: MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder)
MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder) 		1 0 1 3.3E-02 0 0
CUI: C2749106
Disease: Emery-Dreifuss Muscular Dystrophy 6, X-Linked
Emery-Dreifuss Muscular Dystrophy 6, X-Linked 		1 0 1 3.3E-02 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 0 1 3.3E-02 0 0
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 3.3E-02 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 0 1 3.3E-02 0 0
CUI: C2751807
Disease: Emery-Dreifuss Muscular Dystrophy 4
Emery-Dreifuss Muscular Dystrophy 4 		1 0 1 3.3E-02 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 3.3E-02 0 0
CUI: C2930980
Disease: Malignant hyperthermia susceptibility type 1
Malignant hyperthermia susceptibility type 1 		1 0 1 3.3E-02 0 0
CUI: C2931844
Disease: Spinal muscular atrophy 4
Spinal muscular atrophy 4 		1 0 1 3.3E-02 0 0
CUI: C2936171
Disease: Familial Ebstein's Anomaly
Familial Ebstein's Anomaly 		1 0 1 3.3E-02 0 0
CUI: C3150690
Disease: LEFT VENTRICULAR NONCOMPACTION 5
LEFT VENTRICULAR NONCOMPACTION 5 		1 0 1 3.3E-02 0 0
CUI: C3277187
Disease: Type 2 muscle fiber predominance
Type 2 muscle fiber predominance 		1 0 1 3.3E-02 0 0
CUI: C3279722
Disease: MYOPATHY, DISTAL, 4
MYOPATHY, DISTAL, 4 		1 0 1 3.3E-02 0 0
CUI: C3279775
Disease: MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1
MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1 		1 0 1 3.3E-02 0 0
CUI: C3280220
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O 		1 0 1 3.3E-02 0 0
CUI: C3280703
Disease: MYOPATHY, CENTRONUCLEAR, 3
MYOPATHY, CENTRONUCLEAR, 3 		1 0 1 3.3E-02 0 0