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: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 37 10 0.30 14 0.37
CUI: C4021217
Disease: EEG with generalized slow activity
EEG with generalized slow activity 		8 6 2 0.12 2 0.11
CUI: C1849667
Disease: Wide nasal base
Wide nasal base 		12 3 2 9.5E-02 1 5.9E-02
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 9.1E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 9.1E-02 0 0
CUI: C0233283
Disease: Complete breech presentation
Complete breech presentation 		1 1 1 9.1E-02 1 6.7E-02
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 1 1 9.1E-02 1 6.7E-02
CUI: C0242036
Disease: Paraplegia, Ataxic
Paraplegia, Ataxic 		1 0 1 9.1E-02 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 9.1E-02 0 0
CUI: C0278114
Disease: Paraplegia, Cerebral
Paraplegia, Cerebral 		1 0 1 9.1E-02 0 0
CUI: C0278115
Disease: Paraplegia, Spinal
Paraplegia, Spinal 		1 0 1 9.1E-02 0 0
CUI: C0452143
Disease: Paraplegia, Flaccid
Paraplegia, Flaccid 		1 0 1 9.1E-02 0 0
CUI: C0701825
Disease: Acute mastoiditis
Acute mastoiditis 		1 0 1 9.1E-02 0 0
CUI: C0856123
Disease: Myotonia aggravated
Myotonia aggravated 		1 0 1 9.1E-02 0 0
CUI: C1834953
Disease: Lumbar kyphoscoliosis
Lumbar kyphoscoliosis 		1 0 1 9.1E-02 0 0
CUI: C1834961
Disease: Flattened, squared-off epiphyses of tubular bones
Flattened, squared-off epiphyses of tubular bones 		1 0 1 9.1E-02 0 0
CUI: C1835437
Disease: Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type 		1 0 1 9.1E-02 0 0
CUI: C1835442
Disease: Decreased cranial base ossification
Decreased cranial base ossification 		1 0 1 9.1E-02 0 0
CUI: C1835444
Disease: Disc-like vertebral bodies
Disc-like vertebral bodies 		1 0 1 9.1E-02 0 0
CUI: C1835446
Disease: Severe limb shortening
Severe limb shortening 		1 0 1 9.1E-02 0 0
CUI: C1836080
Disease: Stickler Syndrome, Type I, Nonsyndromic Ocular
Stickler Syndrome, Type I, Nonsyndromic Ocular 		1 0 1 9.1E-02 0 0
CUI: C1836081
Disease: RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT
RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT 		1 0 1 9.1E-02 0 0
CUI: C1836683
Disease: Czech dysplasia, metatarsal type
Czech dysplasia, metatarsal type 		1 0 1 9.1E-02 0 0
CUI: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3 		1 0 1 9.1E-02 0 0
CUI: C1851536
Disease: Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness 		1 0 1 9.1E-02 0 0