Source: BEFREE ×
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 14 8 0.14 4 0.16
CUI: C0039743
Disease: Thanatophoric Dysplasia
Thanatophoric Dysplasia 		12 10 7 0.14 4 0.19
CUI: C0343284
Disease: Chondrodysplasia
Chondrodysplasia 		71 0 12 0.11 0 0
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder) 		16 28 6 0.11 3 7.5E-02
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 6.7E-02
CUI: C0410528
Disease: Skeletal dysplasia
Skeletal dysplasia 		87 8 12 9.9E-02 1 4.5E-02
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2 		11 0 5 9.6E-02 0 0
CUI: C0878787
Disease: Growth failure
Growth failure 		83 0 11 9.3E-02 0 0
CUI: C0029422
Disease: Osteochondrodysplasias
Osteochondrodysplasias 		96 8 12 9.2E-02 1 4.5E-02
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis 		14 29 5 9.1E-02 1 2.3E-02
CUI: C3696962
Disease: Coronary microvascular dysfunction
Coronary microvascular dysfunction 		14 0 5 9.1E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		18 0 5 8.5E-02 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related 		31 0 6 8.5E-02 0 0
CUI: C0432211
Disease: Spondyloepimetaphyseal disorder
Spondyloepimetaphyseal disorder 		31 0 6 8.5E-02 0 0
CUI: C0410538
Disease: Pseudoachondroplasia
Pseudoachondroplasia 		19 0 5 8.3E-02 0 0
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism 		21 0 5 8.1E-02 0 0
CUI: C3897045
Disease: Short Stature Homeobox Deficiency
Short Stature Homeobox Deficiency 		8 0 4 8.0E-02 0 0
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency 		91 0 10 7.9E-02 0 0
CUI: C0020514
Disease: Hyperprolactinemia
Hyperprolactinemia 		38 0 6 7.7E-02 0 0
CUI: C0206717
Disease: Olfactory Neuroblastoma
Olfactory Neuroblastoma 		38 0 6 7.7E-02 0 0
CUI: C0265290
Disease: Metaphyseal chondrodysplasia
Metaphyseal chondrodysplasia 		10 0 4 7.7E-02 0 0
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency 		96 0 10 7.6E-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