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: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 4.2E-02 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 4.2E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 4.2E-02 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 4.2E-02 0 0
CUI: C0265201
Disease: De Sanctis-Cacchione syndrome
De Sanctis-Cacchione syndrome 		1 0 1 4.2E-02 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 4.2E-02 0 0
CUI: C0339304
Disease: Neoplasm of cornea
Neoplasm of cornea 		1 0 1 4.2E-02 0 0
CUI: C0342745
Disease: Disorder of galactose metabolism
Disorder of galactose metabolism 		1 0 1 4.2E-02 0 0
CUI: C0393602
Disease: Isolated cervical dystonia
Isolated cervical dystonia 		1 0 1 4.2E-02 0 0
CUI: C0393697
Disease: Epilepsy with grand mal seizures on awakening (disorder)
Epilepsy with grand mal seizures on awakening (disorder) 		1 0 1 4.2E-02 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 4.2E-02 0 0
CUI: C0701825
Disease: Acute mastoiditis
Acute mastoiditis 		1 0 1 4.2E-02 0 0
CUI: C0730364
Disease: Idiopathic polypoidal choroidal vasculopathy
Idiopathic polypoidal choroidal vasculopathy 		1 0 1 4.2E-02 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 4.2E-02 0 0
CUI: C1167779
Disease: Neutropenic infection
Neutropenic infection 		1 0 1 4.2E-02 0 0
CUI: C1392110
Disease: Crystalline cataract
Crystalline cataract 		1 0 1 4.2E-02 0 0
CUI: C1834953
Disease: Lumbar kyphoscoliosis
Lumbar kyphoscoliosis 		1 0 1 4.2E-02 0 0
CUI: C1834961
Disease: Flattened, squared-off epiphyses of tubular bones
Flattened, squared-off epiphyses of tubular bones 		1 0 1 4.2E-02 0 0
CUI: C1835437
Disease: Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type 		1 0 1 4.2E-02 0 0
CUI: C1835442
Disease: Decreased cranial base ossification
Decreased cranial base ossification 		1 0 1 4.2E-02 0 0
CUI: C1835444
Disease: Disc-like vertebral bodies
Disc-like vertebral bodies 		1 0 1 4.2E-02 0 0
CUI: C1835446
Disease: Severe limb shortening
Severe limb shortening 		1 0 1 4.2E-02 0 0
CUI: C1836080
Disease: Stickler Syndrome, Type I, Nonsyndromic Ocular
Stickler Syndrome, Type I, Nonsyndromic Ocular 		1 0 1 4.2E-02 0 0
CUI: C1836081
Disease: RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT
RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT 		1 0 1 4.2E-02 0 0
CUI: C1836683
Disease: Czech dysplasia, metatarsal type
Czech dysplasia, metatarsal type 		1 0 1 4.2E-02 0 0