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: C1969785
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder) 		1 0 1 2.6E-02 0 0
CUI: C2083352
Disease: Rectus femoris muscle atrophy
Rectus femoris muscle atrophy 		1 0 1 2.6E-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 2.6E-02 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve 		1 0 1 2.6E-02 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 0 1 2.6E-02 0 0
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 2.6E-02 0 0
CUI: C2750413
Disease: Cap Myopathy, Tpm2-Related
Cap Myopathy, Tpm2-Related 		1 0 1 2.6E-02 0 0
CUI: C2750414
Disease: CAP MYOPATHY, TPM3-RELATED (disorder)
CAP MYOPATHY, TPM3-RELATED (disorder) 		1 0 1 2.6E-02 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 0 1 2.6E-02 0 0
CUI: C2930980
Disease: Malignant hyperthermia susceptibility type 1
Malignant hyperthermia susceptibility type 1 		1 0 1 2.6E-02 0 0
CUI: C2931004
Disease: Congenital disorder of glycosylation type 1J
Congenital disorder of glycosylation type 1J 		1 0 1 2.6E-02 0 0
CUI: C3150413
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 		1 0 1 2.6E-02 0 0
CUI: C3277187
Disease: Type 2 muscle fiber predominance
Type 2 muscle fiber predominance 		1 0 1 2.6E-02 0 0
CUI: C3279722
Disease: MYOPATHY, DISTAL, 4
MYOPATHY, DISTAL, 4 		1 0 1 2.6E-02 0 0
CUI: C3280220
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O 		1 0 1 2.6E-02 0 0
CUI: C3280679
Disease: MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET 		1 0 1 2.6E-02 0 0
CUI: C3281202
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 13
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 		1 0 1 2.6E-02 0 0
CUI: C3495361
Disease: Gigantiform Cementoma, Familial
Gigantiform Cementoma, Familial 		1 0 1 2.6E-02 0 0
CUI: C3541476
Disease: MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET, MILD VARIANT
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET, MILD VARIANT 		1 0 1 2.6E-02 0 0
CUI: C3542026
Disease: PEROXISOME BIOGENESIS DISORDER 5B
PEROXISOME BIOGENESIS DISORDER 5B 		1 0 1 2.6E-02 0 0
CUI: C3552335
Disease: MYASTHENIC SYNDROME, CONGENITAL, 12
MYASTHENIC SYNDROME, CONGENITAL, 12 		1 0 1 2.6E-02 0 0
CUI: C3553645
Disease: MYASTHENIC SYNDROME, CONGENITAL, 13
MYASTHENIC SYNDROME, CONGENITAL, 13 		1 0 1 2.6E-02 0 0
CUI: C3553656
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB 		1 0 1 2.6E-02 0 0
CUI: C3553940
Disease: PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) 		1 0 1 2.6E-02 0 0
CUI: C3714932
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14 		1 0 1 2.6E-02 0 0