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: C1864853
Disease: Increased vertebral height
Increased vertebral height 		7 1 4 0.29 1 9.1E-02
CUI: C4021386
Disease: Abnormality of the elbow
Abnormality of the elbow 		12 1 4 0.21 1 9.1E-02
CUI: C2678312
Disease: Three M Syndrome 1
Three M Syndrome 1 		2 0 2 0.18 0 0
CUI: C3536734
Disease: Hypoplastic pelvis
Hypoplastic pelvis 		15 2 4 0.18 1 8.3E-02
CUI: C1865030
Disease: Hypoplastic pubic bone
Hypoplastic pubic bone 		10 0 3 0.17 0 0
CUI: C3806510
Disease: Horizontal ribs
Horizontal ribs 		13 0 3 0.14 0 0
CUI: C1859447
Disease: Hypoplastic ischia
Hypoplastic ischia 		14 0 3 0.14 0 0
CUI: C3897045
Disease: Short Stature Homeobox Deficiency
Short Stature Homeobox Deficiency 		8 0 2 0.12 0 0
CUI: C4022001
Disease: Abnormality of the cerebral vasculature
Abnormality of the cerebral vasculature 		18 0 3 0.12 0 0
CUI: C0008449
Disease: Congenital anomaly of cartilage
Congenital anomaly of cartilage 		9 0 2 0.11 0 0
CUI: C1833144
Disease: Slender long bone
Slender long bone 		35 5 4 9.5E-02 3 0.23
CUI: C0936016
Disease: Testicular Feminization
Testicular Feminization 		24 0 3 9.4E-02 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 9.1E-02 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 9.1E-02 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 9.1E-02 0 0
CUI: C0339678
Disease: Simple myopia
Simple myopia 		1 0 1 9.1E-02 0 0
CUI: C0342861
Disease: Uroporphyrinogen decarboxylase deficiency
Uroporphyrinogen decarboxylase deficiency 		1 0 1 9.1E-02 0 0
CUI: C0423693
Disease: Growing pains
Growing pains 		1 0 1 9.1E-02 0 0
CUI: C0748534
Disease: sciatic nerve inflammation
sciatic nerve inflammation 		1 0 1 9.1E-02 0 0
CUI: C1096352
Disease: Pancreatic enlargement
Pancreatic enlargement 		1 0 1 9.1E-02 0 0
CUI: C1851996
Disease: Dwarfism tall vertebrae
Dwarfism tall vertebrae 		1 0 1 9.1E-02 0 0
CUI: C1867968
Disease: Porphyria Cutanea Tarda, Type I
Porphyria Cutanea Tarda, Type I 		1 0 1 9.1E-02 0 0
CUI: C2931631
Disease: Chromosome 7, trisomy mosaic
Chromosome 7, trisomy mosaic 		1 0 1 9.1E-02 0 0
CUI: C2931707
Disease: Chromosome 15, trisomy mosaicism
Chromosome 15, trisomy mosaicism 		1 0 1 9.1E-02 0 0
CUI: C3280146
Disease: THREE M SYNDROME 3
THREE M SYNDROME 3 		1 0 1 9.1E-02 0 0