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: C0265669
Disease: Congenital dislocation of knee
Congenital dislocation of knee 		1 0 1 7.1E-02 0 0
CUI: C0432201
Disease: Boomerang dysplasia
Boomerang dysplasia 		1 0 1 7.1E-02 0 0
CUI: C0432281
Disease: Pseudochondroplasia
Pseudochondroplasia 		1 0 1 7.1E-02 0 0
CUI: C0478074
Disease: Other congenital malformations of spine, not associated with scoliosis
Other congenital malformations of spine, not associated with scoliosis 		1 0 1 7.1E-02 0 0
CUI: C0521527
Disease: Shortened trunk
Shortened trunk 		1 0 1 7.1E-02 0 0
CUI: C0860475
Disease: Lactose intolerant
Lactose intolerant 		1 0 1 7.1E-02 0 0
CUI: C1411006
Disease: Finger contracture
Finger contracture 		1 0 1 7.1E-02 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 0 1 7.1E-02 0 0
CUI: C1838280
Disease: Epiphyseal dysplasia, multiple, 1
Epiphyseal dysplasia, multiple, 1 		1 0 1 7.1E-02 0 0
CUI: C1848473
Disease: Whistling appearance
Whistling appearance 		1 0 1 7.1E-02 0 0
CUI: C1852510
Disease: Craniofacial deafness hand syndrome
Craniofacial deafness hand syndrome 		1 0 1 7.1E-02 0 0
CUI: C1856637
Disease: Spatulate ribs
Spatulate ribs 		1 0 1 7.1E-02 0 0
CUI: C1860309
Disease: Chin with H-shaped crease
Chin with H-shaped crease 		1 0 1 7.1E-02 0 0
CUI: C1862415
Disease: Cervical segmentation defect
Cervical segmentation defect 		1 0 1 7.1E-02 0 0
CUI: C1862420
Disease: Tombstone-shaped proximal phalanges
Tombstone-shaped proximal phalanges 		1 0 1 7.1E-02 0 0
CUI: C1862421
Disease: Widened distal phalanges
Widened distal phalanges 		1 0 1 7.1E-02 0 0
CUI: C1862428
Disease: Thoracic platyspondyly
Thoracic platyspondyly 		1 0 1 7.1E-02 0 0
CUI: C1867440
Disease: Multiple Pterygium Syndrome, Autosomal Dominant
Multiple Pterygium Syndrome, Autosomal Dominant 		1 0 1 7.1E-02 0 0
CUI: C1867494
Disease: Fragmented, irregular epiphyses
Fragmented, irregular epiphyses 		1 0 1 7.1E-02 0 0
CUI: C1968633
Disease: Intimal thickening in the coronary arteries
Intimal thickening in the coronary arteries 		1 0 1 7.1E-02 0 0
CUI: C1968748
Disease: Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement
Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement 		1 0 1 7.1E-02 0 0
CUI: C2678323
Disease: C2-C3 subluxation
C2-C3 subluxation 		1 0 1 7.1E-02 0 0
CUI: C2678399
Disease: Absent humerus
Absent humerus 		1 0 1 7.1E-02 0 0
CUI: C2750413
Disease: Cap Myopathy, Tpm2-Related
Cap Myopathy, Tpm2-Related 		1 0 1 7.1E-02 0 0
CUI: C2751986
Disease: RETINITIS PIGMENTOSA 42
RETINITIS PIGMENTOSA 42 		1 0 1 7.1E-02 0 0