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: C0334483
Disease: Adult rhabdomyoma
Adult rhabdomyoma 		1 0 1 9.1E-02 0 0
CUI: C0403673
Disease: Retrograde ejaculation
Retrograde ejaculation 		1 0 1 9.1E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 9.1E-02 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 9.1E-02 0 0
CUI: C1847532
Disease: MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET
MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET 		1 0 1 9.1E-02 0 0
CUI: C1856697
Disease: Mitochondrial malic enzyme reduced
Mitochondrial malic enzyme reduced 		1 0 1 9.1E-02 0 0
CUI: C1858154
Disease: CARDIOMYOPATHY, DILATED, 1I
CARDIOMYOPATHY, DILATED, 1I 		1 0 1 9.1E-02 0 0
CUI: C1867005
Disease: Scapuloperoneal Syndrome, Neurogenic, Kaeser Type
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type 		1 0 1 9.1E-02 0 0
CUI: C1867451
Disease: Pseudoxanthoma Elasticum, Heterozygous
Pseudoxanthoma Elasticum, Heterozygous 		1 0 1 9.1E-02 0 0
CUI: C1867453
Disease: Peau d'orange retinal changes
Peau d'orange retinal changes 		1 16 1 9.1E-02 7 0.11
CUI: C2033396
Disease: Yellow papule
Yellow papule 		1 0 1 9.1E-02 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 9.1E-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 7 1 9.1E-02 1 1.7E-02
CUI: C3272426
Disease: Gastric Plexiform Fibromyxoma
Gastric Plexiform Fibromyxoma 		1 0 1 9.1E-02 0 0
CUI: C3276161
Disease: ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2 		1 16 1 9.1E-02 9 0.15
CUI: C3277849
Disease: 17,20-Lyase Deficiency, Isolated
17,20-Lyase Deficiency, Isolated 		1 0 1 9.1E-02 0 0
CUI: C3844818
Disease: Attention Deficit Hyper Activity
Attention Deficit Hyper Activity 		1 0 1 9.1E-02 0 0
CUI: C4016476
Disease: DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE
DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE 		1 0 1 9.1E-02 0 0
CUI: C4016477
Disease: INTERMEDIATE MUSCULAR DYSTROPHY
INTERMEDIATE MUSCULAR DYSTROPHY 		1 0 1 9.1E-02 0 0
CUI: C4016970
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 5
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 5 		1 0 1 9.1E-02 0 0
CUI: C4021047
Disease: Impaired visually enhanced vestibulo-ocular reflex
Impaired visually enhanced vestibulo-ocular reflex 		1 0 1 9.1E-02 0 0
CUI: C4022631
Disease: Absent muscle fiber dysferlin
Absent muscle fiber dysferlin 		1 0 1 9.1E-02 0 0
CUI: C4022648
Disease: Abnormal muscle fiber dystrophin expression
Abnormal muscle fiber dystrophin expression 		1 0 1 9.1E-02 0 0
CUI: C4022651
Disease: Reduced muscle fiber merosin
Reduced muscle fiber merosin 		1 0 1 9.1E-02 0 0
CUI: C4022895
Disease: Medial calcification of medium-sized arteries
Medial calcification of medium-sized arteries 		1 0 1 9.1E-02 0 0