Source: INFERRED ×
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: C0018799
Disease: Heart Diseases
Heart Diseases 		1 1 1 9.1E-02 1 1.4E-02
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary 		1 0 1 9.1E-02 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 1 1 9.1E-02 1 1.4E-02
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 3 1 9.1E-02 3 4.1E-02
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 1 1 9.1E-02 1 1.4E-02
CUI: C0340425
Disease: Hypertrophic cardiomyopathy without obstruction
Hypertrophic cardiomyopathy without obstruction 		1 1 1 9.1E-02 1 1.4E-02
CUI: C0343114
Disease: Woolly hair nevus
Woolly hair nevus 		1 0 1 9.1E-02 0 0
CUI: C0348872
Disease: Disorders of both mitral and tricuspid valves
Disorders of both mitral and tricuspid valves 		1 1 1 9.1E-02 1 1.4E-02
CUI: C0410530
Disease: Metachondromatosis
Metachondromatosis 		1 29 1 9.1E-02 19 0.23
CUI: C0442887
Disease: Septal hypertrophy
Septal hypertrophy 		1 1 1 9.1E-02 1 1.4E-02
CUI: C0521579
Disease: Congenital strabismus
Congenital strabismus 		1 0 1 9.1E-02 0 0
CUI: C0544862
Disease: Neurocutaneous melanosis
Neurocutaneous melanosis 		1 0 1 9.1E-02 0 0
CUI: C0578682
Disease: Madarosis of eyebrow
Madarosis of eyebrow 		1 0 1 9.1E-02 0 0
CUI: C0587248
Disease: Costello syndrome (disorder)
Costello syndrome (disorder) 		1 16 1 9.1E-02 1 1.1E-02
CUI: C0700199
Disease: Multiple nevi
Multiple nevi 		1 1 1 9.1E-02 1 1.4E-02
CUI: C1266158
Disease: Nongerminomatous Germ Cell Tumor
Nongerminomatous Germ Cell Tumor 		1 0 1 9.1E-02 0 0
CUI: C1332969
Disease: Childhood Ganglioglioma
Childhood Ganglioglioma 		1 0 1 9.1E-02 0 0
CUI: C1847874
Disease: PHACE association
PHACE association 		1 0 1 9.1E-02 0 0
CUI: C1853120
Disease: Noonan Syndrome 4
Noonan Syndrome 4 		1 8 1 9.1E-02 4 5.2E-02
CUI: C1857534
Disease: Postnatal onset growth deficiency
Postnatal onset growth deficiency 		1 0 1 9.1E-02 0 0
CUI: C1968782
Disease: MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES
MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES 		1 0 1 9.1E-02 0 0
CUI: C1969056
Disease: LEOPARD SYNDROME 2
LEOPARD SYNDROME 2 		1 6 1 9.1E-02 1 1.3E-02
CUI: C1969057
Disease: Noonan Syndrome 5
Noonan Syndrome 5 		1 8 1 9.1E-02 1 1.3E-02
CUI: C2674727
Disease: ASTROCYTOMA, LOW-GRADE, SOMATIC
ASTROCYTOMA, LOW-GRADE, SOMATIC 		1 0 1 9.1E-02 0 0
CUI: C2739810
Disease: Lentigo maligna melanoma
Lentigo maligna melanoma 		1 0 1 9.1E-02 0 0