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 0.33 0 0
CUI: C0024950
Disease: Maxillary Diseases
Maxillary Diseases 		1 0 1 0.33 0 0
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses 		1 0 1 0.33 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea 		1 0 1 0.33 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 0.33 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 0.33 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 0.33 0 0
CUI: C0520474
Disease: Aseptic Necrosis of Bone
Aseptic Necrosis of Bone 		1 0 1 0.33 0 0
CUI: C0701825
Disease: Acute mastoiditis
Acute mastoiditis 		1 0 1 0.33 0 0
CUI: C0741900
Disease: carcinoma sarcoma
carcinoma sarcoma 		1 0 1 0.33 0 0
CUI: C1168331
Disease: Apical myocardial infarction
Apical myocardial infarction 		1 0 1 0.33 0 0
CUI: C1334439
Disease: adenoid cystic carcinoma of lung
adenoid cystic carcinoma of lung 		1 0 1 0.33 0 0
CUI: C1834953
Disease: Lumbar kyphoscoliosis
Lumbar kyphoscoliosis 		1 0 1 0.33 0 0
CUI: C1834961
Disease: Flattened, squared-off epiphyses of tubular bones
Flattened, squared-off epiphyses of tubular bones 		1 0 1 0.33 0 0
CUI: C1835437
Disease: Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type 		1 0 1 0.33 0 0
CUI: C1835442
Disease: Decreased cranial base ossification
Decreased cranial base ossification 		1 0 1 0.33 0 0
CUI: C1835444
Disease: Disc-like vertebral bodies
Disc-like vertebral bodies 		1 0 1 0.33 0 0
CUI: C1835446
Disease: Severe limb shortening
Severe limb shortening 		1 0 1 0.33 0 0
CUI: C1836080
Disease: Stickler Syndrome, Type I, Nonsyndromic Ocular
Stickler Syndrome, Type I, Nonsyndromic Ocular 		1 0 1 0.33 0 0
CUI: C1836081
Disease: RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT
RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT 		1 0 1 0.33 0 0
CUI: C1836683
Disease: Czech dysplasia, metatarsal type
Czech dysplasia, metatarsal type 		1 0 1 0.33 0 0
CUI: C1849011
Disease: SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE
SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE 		1 0 1 0.33 0 0
CUI: C1850158
Disease: Interphalangeal joint erosions
Interphalangeal joint erosions 		1 0 1 0.33 0 0
CUI: C1850159
Disease: Widened metacarpal shaft
Widened metacarpal shaft 		1 0 1 0.33 0 0
CUI: C1850162
Disease: Thin metatarsal cortices
Thin metatarsal cortices 		1 0 1 0.33 0 0