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: C1865847
Disease: Ulnar bowing
Ulnar bowing 		12 0 3 9.4E-02 0 0
CUI: C1842153
Disease: Irregular vertebral endplates
Irregular vertebral endplates 		24 0 4 9.3E-02 0 0
CUI: C0920372
Disease: Carcinogenesis, Radiation
Carcinogenesis, Radiation 		13 0 3 9.1E-02 0 0
CUI: C0029422
Disease: Osteochondrodysplasias
Osteochondrodysplasias 		207 0 19 9.0E-02 0 0
CUI: C0265235
Disease: Marshall syndrome
Marshall syndrome 		2 0 2 8.7E-02 0 0
CUI: C0392476
Disease: Epiphyseal dysplasia
Epiphyseal dysplasia 		27 0 4 8.7E-02 0 0
CUI: C0877550
Disease: Carcinomatous ascites
Carcinomatous ascites 		2 0 2 8.7E-02 0 0
CUI: C4025050
Disease: Irregular distal femoral epiphysis
Irregular distal femoral epiphysis 		2 0 2 8.7E-02 0 0
CUI: C4025356
Disease: Abnormal vitreous humor morphology
Abnormal vitreous humor morphology 		2 0 2 8.7E-02 0 0
CUI: C4479260
Disease: AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2
AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2 		2 0 2 8.7E-02 0 0
CUI: C4551562
Disease: AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 1
AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 1 		2 0 2 8.7E-02 0 0
CUI: C4688354
Disease: Recurrent Craniopharyngioma
Recurrent Craniopharyngioma 		2 0 2 8.7E-02 0 0
CUI: C0409345
Disease: Flexion contracture - wrist
Flexion contracture - wrist 		15 0 3 8.6E-02 0 0
CUI: C1846449
Disease: Irregular epiphyses
Irregular epiphyses 		15 0 3 8.6E-02 0 0
CUI: C0026707
Disease: Mucopolysaccharidosis IV
Mucopolysaccharidosis IV 		28 0 4 8.5E-02 0 0
CUI: C0014761
Disease: Erythroblastosis, Fetal
Erythroblastosis, Fetal 		16 0 3 8.3E-02 0 0
CUI: C0155366
Disease: Vitreous degeneration
Vitreous degeneration 		3 0 2 8.3E-02 0 0
CUI: C0524595
Disease: Aseptic Necrosis of Femur Head
Aseptic Necrosis of Femur Head 		3 0 2 8.3E-02 0 0
CUI: C1844509
Disease: Antegonial notching of mandible
Antegonial notching of mandible 		3 0 2 8.3E-02 0 0
CUI: C1848488
Disease: Pierre Robin syndrome with fetal chondrodysplasia
Pierre Robin syndrome with fetal chondrodysplasia 		3 0 2 8.3E-02 0 0
CUI: C1856780
Disease: Posterior vertebral hypoplasia
Posterior vertebral hypoplasia 		3 0 2 8.3E-02 0 0
CUI: C1860601
Disease: Flattened femoral head
Flattened femoral head 		3 0 2 8.3E-02 0 0
CUI: C1861218
Disease: Hypoplastic ilia
Hypoplastic ilia 		16 0 3 8.3E-02 0 0
CUI: C4476938
Disease: Impairment of activities of daily living
Impairment of activities of daily living 		3 0 2 8.3E-02 0 0
CUI: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia 		16 0 3 8.3E-02 0 0