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 4.5E-02 0 0
CUI: C0042907
Disease: Vitreous Detachment
Vitreous Detachment 		1 0 1 4.5E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 4.5E-02 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 1 1 4.5E-02 1 0.50
CUI: C0233480
Disease: Hyperirritability
Hyperirritability 		1 0 1 4.5E-02 0 0
CUI: C0268016
Disease: Chronic hypokalemia
Chronic hypokalemia 		1 0 1 4.5E-02 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 4.5E-02 0 0
CUI: C0521668
Disease: Primary Thunderclap Headache
Primary Thunderclap Headache 		1 0 1 4.5E-02 0 0
CUI: C0685108
Disease: Lenegre's disease
Lenegre's disease 		1 0 1 4.5E-02 0 0
CUI: C0685661
Disease: Congenital anomaly of ischium
Congenital anomaly of ischium 		1 1 1 4.5E-02 1 0.50
CUI: C0701825
Disease: Acute mastoiditis
Acute mastoiditis 		1 0 1 4.5E-02 0 0
CUI: C0748694
Disease: sick sinus
sick sinus 		1 0 1 4.5E-02 0 0
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E 		1 0 1 4.5E-02 0 0
CUI: C1833154
Disease: Long Qt Syndrome 4
Long Qt Syndrome 4 		1 0 1 4.5E-02 0 0
CUI: C1833236
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder) 		1 0 1 4.5E-02 0 0
CUI: C1834144
Disease: Sick Sinus Syndrome 2, Autosomal Dominant
Sick Sinus Syndrome 2, Autosomal Dominant 		1 0 1 4.5E-02 0 0
CUI: C1834953
Disease: Lumbar kyphoscoliosis
Lumbar kyphoscoliosis 		1 0 1 4.5E-02 0 0
CUI: C1834961
Disease: Flattened, squared-off epiphyses of tubular bones
Flattened, squared-off epiphyses of tubular bones 		1 0 1 4.5E-02 0 0
CUI: C1835437
Disease: Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type 		1 0 1 4.5E-02 0 0
CUI: C1835442
Disease: Decreased cranial base ossification
Decreased cranial base ossification 		1 0 1 4.5E-02 0 0
CUI: C1835444
Disease: Disc-like vertebral bodies
Disc-like vertebral bodies 		1 0 1 4.5E-02 0 0
CUI: C1835446
Disease: Severe limb shortening
Severe limb shortening 		1 0 1 4.5E-02 0 0
CUI: C1836080
Disease: Stickler Syndrome, Type I, Nonsyndromic Ocular
Stickler Syndrome, Type I, Nonsyndromic Ocular 		1 0 1 4.5E-02 0 0
CUI: C1836081
Disease: RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT
RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT 		1 0 1 4.5E-02 0 0
CUI: C1836683
Disease: Czech dysplasia, metatarsal type
Czech dysplasia, metatarsal type 		1 0 1 4.5E-02 0 0