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: C4017222
Disease: FACTOR XII (LOCARNO) PHENOTYPE
FACTOR XII (LOCARNO) PHENOTYPE 		2 0 2 0.18 0 0
CUI: C2697764
Disease: Interleukin 16 Measurement
Interleukin 16 Measurement 		9 0 3 0.18 0 0
CUI: C1857728
Disease: Hereditary Angioedema Type III
Hereditary Angioedema Type III 		4 0 2 0.15 0 0
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		17 0 3 0.12 0 0
CUI: C0272334
Disease: Hereditary factor XII deficiency disease
Hereditary factor XII deficiency disease 		1 0 1 9.1E-02 0 0
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia 		1 0 1 9.1E-02 0 0
CUI: C0744314
Disease: Gastroenterocolitis
Gastroenterocolitis 		1 0 1 9.1E-02 0 0
CUI: C1960459
Disease: Hereditary angioedema with normal C1 esterase inhibitor activity
Hereditary angioedema with normal C1 esterase inhibitor activity 		1 0 1 9.1E-02 0 0
CUI: C1969785
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder) 		1 0 1 9.1E-02 0 0
CUI: C3495361
Disease: Gigantiform Cementoma, Familial
Gigantiform Cementoma, Familial 		1 0 1 9.1E-02 0 0
CUI: C4022978
Disease: Episodic upper airway obstruction
Episodic upper airway obstruction 		1 0 1 9.1E-02 0 0
CUI: C4225292
Disease: THYROID CANCER, NONMEDULLARY, 5
THYROID CANCER, NONMEDULLARY, 5 		1 1 1 9.1E-02 1 7.1E-02
CUI: C4552292
Disease: Hereditary angioedema with normal C1 esterase inhibitor
Hereditary angioedema with normal C1 esterase inhibitor 		1 0 1 9.1E-02 0 0
CUI: C4727977
Disease: Hospital acquired bacterial pneumonia
Hospital acquired bacterial pneumonia 		1 0 1 9.1E-02 0 0
CUI: C0015526
Disease: Factor XII Deficiency
Factor XII Deficiency 		14 0 2 8.7E-02 0 0
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding) 		14 0 2 8.7E-02 0 0
CUI: C0236024
Disease: Edema of pharynx
Edema of pharynx 		2 0 1 8.3E-02 0 0
CUI: C0586738
Disease: Calf muscle weakness
Calf muscle weakness 		2 0 1 8.3E-02 0 0
CUI: C1142262
Disease: Intestinal edema
Intestinal edema 		2 0 1 8.3E-02 0 0
CUI: C1833739
Disease: Diaphyseal cortical sclerosis
Diaphyseal cortical sclerosis 		2 0 1 8.3E-02 0 0
CUI: C2189270
Disease: VABP
VABP 		2 0 1 8.3E-02 0 0
CUI: C2750076
Disease: Miyoshi Muscular Dystrophy 3
Miyoshi Muscular Dystrophy 3 		2 0 1 8.3E-02 0 0
CUI: C4551981
Disease: Familial Multiple Coagulation Factor Deficiency I
Familial Multiple Coagulation Factor Deficiency I 		2 0 1 8.3E-02 0 0
CUI: C1290708
Disease: Osteomyelitis of mandible
Osteomyelitis of mandible 		3 0 1 7.7E-02 0 0
CUI: C2873785
Disease: Deficiency of factor V [labile]
Deficiency of factor V [labile] 		3 0 1 7.7E-02 0 0