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: C1865030
Disease: Hypoplastic pubic bone
Hypoplastic pubic bone 		10 0 7 0.41 0 0
CUI: C1861218
Disease: Hypoplastic ilia
Hypoplastic ilia 		16 0 6 0.25 0 0
CUI: C1846434
Disease: Hypoplastic scapulae
Hypoplastic scapulae 		18 0 6 0.23 0 0
CUI: C1837082
Disease: Metaphyseal cupping
Metaphyseal cupping 		13 0 5 0.23 0 0
CUI: C1848488
Disease: Pierre Robin syndrome with fetal chondrodysplasia
Pierre Robin syndrome with fetal chondrodysplasia 		3 0 3 0.21 0 0
CUI: C1858084
Disease: STICKLER SYNDROME, TYPE II (disorder)
STICKLER SYNDROME, TYPE II (disorder) 		4 0 3 0.20 0 0
CUI: C2749582
Disease: Dumbbell-shaped long bone
Dumbbell-shaped long bone 		4 0 3 0.20 0 0
CUI: C1850293
Disease: Severe platyspondyly
Severe platyspondyly 		5 0 3 0.19 0 0
CUI: C1865186
Disease: Bell-shaped thorax
Bell-shaped thorax 		26 0 6 0.18 0 0
CUI: C3806510
Disease: Horizontal ribs
Horizontal ribs 		13 0 4 0.17 0 0
CUI: C1864853
Disease: Increased vertebral height
Increased vertebral height 		7 0 3 0.17 0 0
CUI: C3536734
Disease: Hypoplastic pelvis
Hypoplastic pelvis 		15 0 4 0.16 0 0
CUI: C1854928
Disease: Protuberant abdomen
Protuberant abdomen 		25 0 5 0.15 0 0
CUI: C4020962
Disease: Enlarged thorax
Enlarged thorax 		25 0 5 0.15 0 0
CUI: C0265235
Disease: Marshall syndrome
Marshall syndrome 		2 0 2 0.14 0 0
CUI: C1846154
Disease: Anterior rib cupping
Anterior rib cupping 		10 0 3 0.14 0 0
CUI: C1855310
Disease: Megaepiphyseal dwarfism
Megaepiphyseal dwarfism 		2 0 2 0.14 0 0
CUI: C1861481
Disease: Stickler syndrome, type 3
Stickler syndrome, type 3 		2 0 2 0.14 0 0
CUI: C2678312
Disease: Three M Syndrome 1
Three M Syndrome 1 		2 0 2 0.14 0 0
CUI: C4025356
Disease: Abnormal vitreous humor morphology
Abnormal vitreous humor morphology 		2 0 2 0.14 0 0
CUI: C1834954
Disease: Coronal cleft vertebrae
Coronal cleft vertebrae 		11 0 3 0.14 0 0
CUI: C1848862
Disease: Miller-McKusick-Malvaux-Syndrome (3M Syndrome)
Miller-McKusick-Malvaux-Syndrome (3M Syndrome) 		11 0 3 0.14 0 0
CUI: C4021787
Disease: Abnormal diaphysis morphology
Abnormal diaphysis morphology 		11 0 3 0.14 0 0
CUI: C0155366
Disease: Vitreous degeneration
Vitreous degeneration 		3 0 2 0.13 0 0
CUI: C0265282
Disease: Fibrochondrogenesis
Fibrochondrogenesis 		3 0 2 0.13 0 0