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 7.1E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly
1 0 1 7.1E-02 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation
1 0 1 7.1E-02 0 0
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A
1 0 1 7.1E-02 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A
1 0 1 7.1E-02 0 0
CUI: C0432219
Disease: Opsismodysplasia
Opsismodysplasia
1 0 1 7.1E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia
1 0 1 7.1E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis
1 0 1 7.1E-02 0 0
CUI: C0701825
Disease: Acute mastoiditis
Acute mastoiditis
1 0 1 7.1E-02 0 0
CUI: C0743924
Disease: Short fetal femur length
Short fetal femur length
1 0 1 7.1E-02 0 0
CUI: C1389473
Disease: Pelvic hypoplasia
Pelvic hypoplasia
1 0 1 7.1E-02 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma
1 0 1 7.1E-02 0 0
Estrogen Receptor Status - Clinical Trial Eligibility Criteria
1 0 1 7.1E-02 0 0
Cervical Keratinizing Squamous Cell Carcinoma
1 0 1 7.1E-02 0 0
CUI: C1834953
Disease: Lumbar kyphoscoliosis
Lumbar kyphoscoliosis
1 0 1 7.1E-02 0 0
Flattened, squared-off epiphyses of tubular bones
1 0 1 7.1E-02 0 0
CUI: C1835101
Disease: Wide tufts of distal phalanges
Wide tufts of distal phalanges
1 0 1 7.1E-02 0 0
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
1 0 1 7.1E-02 0 0
CUI: C1835442
Disease: Decreased cranial base ossification
Decreased cranial base ossification
1 0 1 7.1E-02 0 0
CUI: C1835444
Disease: Disc-like vertebral bodies
Disc-like vertebral bodies
1 0 1 7.1E-02 0 0
CUI: C1835446
Disease: Severe limb shortening
Severe limb shortening
1 0 1 7.1E-02 0 0
Stickler Syndrome, Type I, Nonsyndromic Ocular
1 0 1 7.1E-02 0 0
RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT
1 0 1 7.1E-02 0 0
CUI: C1836683
Disease: Czech dysplasia, metatarsal type
Czech dysplasia, metatarsal type
1 0 1 7.1E-02 0 0
CUI: C1850040
Disease: Pelviscapular dysplasia
Pelviscapular dysplasia
1 0 1 7.1E-02 0 0