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: C1861218
Disease: Hypoplastic ilia
Hypoplastic ilia 		16 0 6 0.17 0 0
CUI: C1837482
Disease: Thoracic hypoplasia
Thoracic hypoplasia 		32 0 8 0.16 0 0
CUI: C1846434
Disease: Hypoplastic scapulae
Hypoplastic scapulae 		18 0 6 0.16 0 0
CUI: C1837082
Disease: Metaphyseal cupping
Metaphyseal cupping 		13 0 5 0.15 0 0
CUI: C1865200
Disease: Delayed epiphyseal ossification
Delayed epiphyseal ossification 		13 0 5 0.15 0 0
CUI: C1837485
Disease: Flat acetabular roof
Flat acetabular roof 		21 0 6 0.15 0 0
CUI: C1859447
Disease: Hypoplastic ischia
Hypoplastic ischia 		14 0 5 0.15 0 0
CUI: C0595939
Disease: Stillbirth
Stillbirth 		23 0 6 0.14 0 0
CUI: C1866730
Disease: Rhizomelia
Rhizomelia 		57 0 10 0.14 0 0
CUI: C1854912
Disease: Short long bone
Short long bone 		42 0 8 0.14 0 0
CUI: C0426817
Disease: Short ribs
Short ribs 		60 0 10 0.13 0 0
CUI: C1846435
Disease: Disproportionate short-trunk short stature
Disproportionate short-trunk short stature 		19 0 5 0.13 0 0
CUI: C1834954
Disease: Coronal cleft vertebrae
Coronal cleft vertebrae 		11 0 4 0.12 0 0
CUI: C4021787
Disease: Abnormal diaphysis morphology
Abnormal diaphysis morphology 		11 0 4 0.12 0 0
CUI: C1848488
Disease: Pierre Robin syndrome with fetal chondrodysplasia
Pierre Robin syndrome with fetal chondrodysplasia 		3 0 3 0.12 0 0
CUI: C4476534
Disease: Subperiosteal bone resorption
Subperiosteal bone resorption 		3 0 3 0.12 0 0
CUI: C0001079
Disease: Achondrogenesis
Achondrogenesis 		4 0 3 0.12 0 0
CUI: C1838659
Disease: Deformed rib cage
Deformed rib cage 		4 0 3 0.12 0 0
CUI: C1848538
Disease: Bulging of the costochondral junction
Bulging of the costochondral junction 		4 0 3 0.12 0 0
CUI: C1858084
Disease: STICKLER SYNDROME, TYPE II (disorder)
STICKLER SYNDROME, TYPE II (disorder) 		4 0 3 0.12 0 0
CUI: C2749582
Disease: Dumbbell-shaped long bone
Dumbbell-shaped long bone 		4 0 3 0.12 0 0
CUI: C4025628
Disease: Abnormal enchondral ossification
Abnormal enchondral ossification 		4 0 3 0.12 0 0
CUI: C1833325
Disease: Thin bony cortex
Thin bony cortex 		14 0 4 0.11 0 0
CUI: C1838662
Disease: Metaphyseal irregularity
Metaphyseal irregularity 		34 0 6 0.11 0 0
CUI: C1833324
Disease: Sparse bone trabeculae
Sparse bone trabeculae 		5 0 3 0.11 0 0