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: C0031925
Disease: Pilonidal Cyst
Pilonidal Cyst 		1 0 1 5.6E-02 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 5.6E-02 0 0
CUI: C0201896
Disease: Arylsulfatase B measurement
Arylsulfatase B measurement 		1 0 1 5.6E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 5.6E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 5.6E-02 0 0
CUI: C0268218
Disease: Maroteaux-Lamy syndrome, mild form
Maroteaux-Lamy syndrome, mild form 		1 0 1 5.6E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 5.6E-02 0 0
CUI: C0332778
Disease: Diastasis, Bone
Diastasis, Bone 		1 0 1 5.6E-02 0 0
CUI: C0409579
Disease: Rheumatic joint disease
Rheumatic joint disease 		1 0 1 5.6E-02 0 0
CUI: C0432268
Disease: Osteopathia striata cranial sclerosis
Osteopathia striata cranial sclerosis 		1 0 1 5.6E-02 0 0
CUI: C0432269
Disease: Lenz Majewski hyperostotic dwarfism
Lenz Majewski hyperostotic dwarfism 		1 0 1 5.6E-02 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 5.6E-02 0 0
CUI: C0796280
Disease: Acromegaloid facial appearance syndrome
Acromegaloid facial appearance syndrome 		1 0 1 5.6E-02 0 0
CUI: C0840564
Disease: Rupture of bladder
Rupture of bladder 		1 0 1 5.6E-02 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 5.6E-02 0 0
CUI: C0865573
Disease: Mitral disease
Mitral disease 		1 0 1 5.6E-02 0 0
CUI: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection 		1 0 1 5.6E-02 0 0
CUI: C1303076
Disease: Tortuous carotid artery
Tortuous carotid artery 		1 0 1 5.6E-02 0 0
CUI: C1832942
Disease: JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder) 		1 0 1 5.6E-02 0 0
CUI: C1835101
Disease: Wide tufts of distal phalanges
Wide tufts of distal phalanges 		1 0 1 5.6E-02 0 0
CUI: C1835130
Disease: Premature calcification of mitral annulus
Premature calcification of mitral annulus 		1 0 1 5.6E-02 0 0
CUI: C1835470
Disease: Progressive sclerosis of skull base
Progressive sclerosis of skull base 		1 0 1 5.6E-02 0 0
CUI: C1837839
Disease: CARDIOMYOPATHY, DILATED, 1O
CARDIOMYOPATHY, DILATED, 1O 		1 0 1 5.6E-02 0 0
CUI: C1848651
Disease: Al Awadi syndrome
Al Awadi syndrome 		1 0 1 5.6E-02 0 0
CUI: C1848653
Disease: Anteriorly displaced genitalia
Anteriorly displaced genitalia 		1 0 1 5.6E-02 0 0