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: C1855240
Disease: Irregular tarsal bones
Irregular tarsal bones 		1 0 1 5.9E-02 0 0
CUI: C1866075
Disease: GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder) 		1 0 1 5.9E-02 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 5.9E-02 0 0
CUI: C2937300
Disease: Congenital hereditary muscular dystrophy
Congenital hereditary muscular dystrophy 		1 0 1 5.9E-02 0 0
CUI: C3179037
Disease: Developmental Coxa Vara
Developmental Coxa Vara 		1 0 1 5.9E-02 0 0
CUI: C3805692
Disease: Hyperpigmented nevi and streak
Hyperpigmented nevi and streak 		1 0 1 5.9E-02 0 0
CUI: C3806511
Disease: Horizontal inferior border of scapula
Horizontal inferior border of scapula 		1 0 1 5.9E-02 0 0
CUI: C3844818
Disease: Attention Deficit Hyper Activity
Attention Deficit Hyper Activity 		1 0 1 5.9E-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 5.9E-02 0 0
CUI: C4016477
Disease: INTERMEDIATE MUSCULAR DYSTROPHY
INTERMEDIATE MUSCULAR DYSTROPHY 		1 0 1 5.9E-02 0 0
CUI: C4017296
Disease: VON WILLEBRAND DISEASE, TYPE 1, SUSCEPTIBILITY TO
VON WILLEBRAND DISEASE, TYPE 1, SUSCEPTIBILITY TO 		1 0 1 5.9E-02 0 0
CUI: C4017650
Disease: VON WILLEBRAND FACTOR VICENZA PHENOTYPE
VON WILLEBRAND FACTOR VICENZA PHENOTYPE 		1 0 1 5.9E-02 0 0
CUI: C4021055
Disease: Absent muscle fiber merosin
Absent muscle fiber merosin 		1 0 1 5.9E-02 0 0
CUI: C4021108
Disease: Anterior wedging of T12
Anterior wedging of T12 		1 0 1 5.9E-02 0 0
CUI: C4021652
Disease: Anterior wedging of T11
Anterior wedging of T11 		1 0 1 5.9E-02 0 0
CUI: C4022648
Disease: Abnormal muscle fiber dystrophin expression
Abnormal muscle fiber dystrophin expression 		1 0 1 5.9E-02 0 0
CUI: C4024620
Disease: Widened sacrosciatic notch
Widened sacrosciatic notch 		1 0 1 5.9E-02 0 0
CUI: C4025053
Disease: Broad long bone diaphyses
Broad long bone diaphyses 		1 0 1 5.9E-02 0 0
CUI: C4025255
Disease: Cone-shaped epiphyses fused within their metaphyses
Cone-shaped epiphyses fused within their metaphyses 		1 0 1 5.9E-02 0 0
CUI: C4025262
Disease: Prominent styloid process of ulna
Prominent styloid process of ulna 		1 0 1 5.9E-02 0 0
CUI: C4025275
Disease: Generalized distal tubular acidosis
Generalized distal tubular acidosis 		1 0 1 5.9E-02 0 0
CUI: C4025307
Disease: Hyperconvex vertebral body endplates
Hyperconvex vertebral body endplates 		1 0 1 5.9E-02 0 0
CUI: C4025457
Disease: Cone-shaped distal radial epiphysis
Cone-shaped distal radial epiphysis 		1 0 1 5.9E-02 0 0
CUI: C4025733
Disease: Mesangial abnormality
Mesangial abnormality 		1 0 1 5.9E-02 0 0
CUI: C4225313
Disease: BETHLEM MYOPATHY 2
BETHLEM MYOPATHY 2 		1 0 1 5.9E-02 0 0