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 4.0E-02 0 0
CUI: C0036413
Disease: Scleredema Adultorum
Scleredema Adultorum 		1 0 1 4.0E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 4.0E-02 0 0
CUI: C0038557
Disease: Submandibular Gland Diseases
Submandibular Gland Diseases 		1 0 1 4.0E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 4.0E-02 0 0
CUI: C0201896
Disease: Arylsulfatase B measurement
Arylsulfatase B measurement 		1 0 1 4.0E-02 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 4.0E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 4.0E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 4.0E-02 0 0
CUI: C0268218
Disease: Maroteaux-Lamy syndrome, mild form
Maroteaux-Lamy syndrome, mild form 		1 0 1 4.0E-02 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 4.0E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 4.0E-02 0 0
CUI: C0343263
Disease: Chondrolysis of articular cartilage
Chondrolysis of articular cartilage 		1 0 1 4.0E-02 0 0
CUI: C0432281
Disease: Pseudochondroplasia
Pseudochondroplasia 		1 0 1 4.0E-02 0 0
CUI: C0495617
Disease: Congenital scoliosis due to bony malformation
Congenital scoliosis due to bony malformation 		1 0 1 4.0E-02 0 0
CUI: C0521527
Disease: Shortened trunk
Shortened trunk 		1 0 1 4.0E-02 0 0
CUI: C0523633
Disease: Fibronectin measurement
Fibronectin measurement 		1 0 1 4.0E-02 0 0
CUI: C0575827
Disease: Small finger
Small finger 		1 0 1 4.0E-02 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 4.0E-02 0 0
CUI: C0701825
Disease: Acute mastoiditis
Acute mastoiditis 		1 0 1 4.0E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 4.0E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 4.0E-02 0 0
CUI: C0796280
Disease: Acromegaloid facial appearance syndrome
Acromegaloid facial appearance syndrome 		1 0 1 4.0E-02 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 4.0E-02 0 0
CUI: C0853856
Disease: Staphylococcal abscess
Staphylococcal abscess 		1 0 1 4.0E-02 0 0