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: C1868678
Disease: THANATOPHORIC DYSPLASIA, TYPE I (disorder)
THANATOPHORIC DYSPLASIA, TYPE I (disorder) 		20 18 8 0.14 9 0.30
CUI: C0039743
Disease: Thanatophoric Dysplasia
Thanatophoric Dysplasia 		12 10 7 0.14 6 0.24
CUI: C0343284
Disease: Chondrodysplasia
Chondrodysplasia 		71 0 12 0.11 0 0
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder) 		16 42 6 0.11 9 0.17
CUI: C0265290
Disease: Metaphyseal chondrodysplasia
Metaphyseal chondrodysplasia 		20 0 6 1.0E-01 0 0
CUI: C0271568
Disease: Laron Syndrome
Laron Syndrome 		20 0 6 1.0E-01 0 0
CUI: C0744483
Disease: growth hormone treatment
growth hormone treatment 		20 1 6 1.0E-01 1 4.8E-02
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2 		11 17 5 9.6E-02 8 0.27
CUI: C0878787
Disease: Growth failure
Growth failure 		84 0 11 9.2E-02 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis 		14 29 5 9.1E-02 2 4.2E-02
CUI: C3696962
Disease: Coronary microvascular dysfunction
Coronary microvascular dysfunction 		14 0 5 9.1E-02 0 0
CUI: C0410538
Disease: Pseudoachondroplasia
Pseudoachondroplasia 		19 0 5 8.3E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 24 5 8.2E-02 1 2.3E-02
CUI: C3897045
Disease: Short Stature Homeobox Deficiency
Short Stature Homeobox Deficiency 		8 0 4 8.0E-02 0 0
CUI: C0432211
Disease: Spondyloepimetaphyseal disorder
Spondyloepimetaphyseal disorder 		37 0 6 7.8E-02 0 0
CUI: C0206717
Disease: Olfactory Neuroblastoma
Olfactory Neuroblastoma 		38 0 6 7.7E-02 0 0
CUI: C3899655
Disease: Childhood Langerhans Cell Histiocytosis
Childhood Langerhans Cell Histiocytosis 		40 0 6 7.5E-02 0 0
CUI: C3900100
Disease: Adult Langerhans Cell Histiocytosis
Adult Langerhans Cell Histiocytosis 		40 0 6 7.5E-02 0 0
CUI: C0027719
Disease: Nephrosclerosis
Nephrosclerosis 		41 0 6 7.4E-02 0 0
CUI: C0026707
Disease: Mucopolysaccharidosis IV
Mucopolysaccharidosis IV 		28 0 5 7.2E-02 0 0
CUI: C1837475
Disease: Insulin-Like Growth Factor I Deficiency
Insulin-Like Growth Factor I Deficiency 		28 0 5 7.2E-02 0 0
CUI: C1857941
Disease: Brooke-Spiegler syndrome
Brooke-Spiegler syndrome 		45 0 6 7.1E-02 0 0
CUI: C2931196
Disease: Craniofacial dysostosis type 1
Craniofacial dysostosis type 1 		15 52 4 7.0E-02 2 2.8E-02
CUI: C2745963
Disease: Kashin-Beck Disease
Kashin-Beck Disease 		77 0 8 7.0E-02 0 0
CUI: C0333291
Disease: Bleeding ulcer
Bleeding ulcer 		16 0 4 6.9E-02 0 0