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: C0426801
Disease: Broad clavicle
Broad clavicle 		9 0 4 0.17 0 0
CUI: C4024618
Disease: Large iliac wings
Large iliac wings 		6 0 3 0.14 0 0
CUI: C1855665
Disease: Ovoid vertebral bodies
Ovoid vertebral bodies 		25 0 5 0.13 0 0
CUI: C1858452
Disease: Thickened calvaria
Thickened calvaria 		27 0 5 0.12 0 0
CUI: C1865244
Disease: Shallow orbits
Shallow orbits 		20 0 4 0.12 0 0
CUI: C0241165
Disease: Thick skin
Thick skin 		40 0 6 0.12 0 0
CUI: C1849305
Disease: Aplasia/Hypoplasia of the pubic bone
Aplasia/Hypoplasia of the pubic bone 		2 0 2 0.11 0 0
CUI: C1854912
Disease: Short long bone
Short long bone 		42 0 6 0.11 0 0
CUI: C2673653
Disease: Cuboid-shaped vertebral bodies
Cuboid-shaped vertebral bodies 		2 0 2 0.11 0 0
CUI: C1849039
Disease: Metaphyseal widening
Metaphyseal widening 		43 0 6 0.11 0 0
CUI: C0265282
Disease: Fibrochondrogenesis
Fibrochondrogenesis 		3 0 2 0.11 0 0
CUI: C0424693
Disease: Broad skull
Broad skull 		3 0 2 0.11 0 0
CUI: C1843677
Disease: Large sella turcica
Large sella turcica 		3 0 2 0.11 0 0
CUI: C1848488
Disease: Pierre Robin syndrome with fetal chondrodysplasia
Pierre Robin syndrome with fetal chondrodysplasia 		3 0 2 0.11 0 0
CUI: C1869114
Disease: Weill-Marchesani Syndrome, Autosomal Recessive
Weill-Marchesani Syndrome, Autosomal Recessive 		3 0 2 0.11 0 0
CUI: C1869115
Disease: Weill-Marchesani Syndrome, Autosomal Dominant
Weill-Marchesani Syndrome, Autosomal Dominant 		3 0 2 0.11 0 0
CUI: C4025193
Disease: Craniofacial osteosclerosis
Craniofacial osteosclerosis 		3 0 2 0.11 0 0
CUI: C0584837
Disease: Choanal stenosis
Choanal stenosis 		14 0 3 0.10 0 0
CUI: C0238669
Disease: Aortic root dilatation
Aortic root dilatation 		15 0 3 1.0E-01 0 0
CUI: C0795905
Disease: Cantu syndrome
Cantu syndrome 		4 0 2 1.0E-01 0 0
CUI: C1857501
Disease: Facial hyperostosis
Facial hyperostosis 		4 0 2 1.0E-01 0 0
CUI: C1858084
Disease: STICKLER SYNDROME, TYPE II (disorder)
STICKLER SYNDROME, TYPE II (disorder) 		4 0 2 1.0E-01 0 0
CUI: C4021391
Disease: Broad phalanges of the hand
Broad phalanges of the hand 		4 0 2 1.0E-01 0 0
CUI: C4021738
Disease: Abnormality of the pubic bone
Abnormality of the pubic bone 		4 0 2 1.0E-01 0 0
CUI: C0392476
Disease: Epiphyseal dysplasia
Epiphyseal dysplasia 		27 0 4 9.8E-02 0 0