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: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1 		11 73 4 0.33 1 1.3E-02
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		4 70 2 0.29 1 1.4E-02
CUI: C0206729
Disease: Neurofibrosarcoma
Neurofibrosarcoma 		5 0 2 0.25 0 0
CUI: C1864795
Disease: Superior pectus carinatum
Superior pectus carinatum 		5 0 2 0.25 0 0
CUI: C1864796
Disease: Pectus excavatum of inferior sternum
Pectus excavatum of inferior sternum 		5 0 2 0.25 0 0
CUI: C4024692
Disease: Reduced factor XIII activity
Reduced factor XIII activity 		5 0 2 0.25 0 0
CUI: C4025759
Disease: Abnormal mitral valve morphology
Abnormal mitral valve morphology 		5 0 2 0.25 0 0
CUI: C0015526
Disease: Factor XII Deficiency
Factor XII Deficiency 		6 0 2 0.22 0 0
CUI: C0039103
Disease: Synovitis
Synovitis 		6 0 2 0.22 0 0
CUI: C0398639
Disease: Amegakaryocytic thrombocytopenia
Amegakaryocytic thrombocytopenia 		6 0 2 0.22 0 0
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		12 153 3 0.21 2 1.3E-02
CUI: C0265338
Disease: Coffin-Siris syndrome
Coffin-Siris syndrome 		1 0 1 0.20 0 0
CUI: C0521579
Disease: Congenital strabismus
Congenital strabismus 		1 0 1 0.20 0 0
CUI: C0578682
Disease: Madarosis of eyebrow
Madarosis of eyebrow 		1 0 1 0.20 0 0
CUI: C1266158
Disease: Nongerminomatous Germ Cell Tumor
Nongerminomatous Germ Cell Tumor 		1 0 1 0.20 0 0
CUI: C1332969
Disease: Childhood Ganglioglioma
Childhood Ganglioglioma 		1 0 1 0.20 0 0
CUI: C1847874
Disease: PHACE association
PHACE association 		1 0 1 0.20 0 0
CUI: C1851095
Disease: Lumbosacral hirsutism
Lumbosacral hirsutism 		1 1 1 0.20 1 0.33
CUI: C1857534
Disease: Postnatal onset growth deficiency
Postnatal onset growth deficiency 		1 0 1 0.20 0 0
CUI: C2674727
Disease: ASTROCYTOMA, LOW-GRADE, SOMATIC
ASTROCYTOMA, LOW-GRADE, SOMATIC 		1 0 1 0.20 0 0
CUI: C2739810
Disease: Lentigo maligna melanoma
Lentigo maligna melanoma 		1 0 1 0.20 0 0
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		1 0 1 0.20 0 0
CUI: C3150971
Disease: LEOPARD SYNDROME 3
LEOPARD SYNDROME 3 		1 0 1 0.20 0 0
CUI: C3809006
Disease: CARDIOFACIOCUTANEOUS SYNDROME 3
CARDIOFACIOCUTANEOUS SYNDROME 3 		1 0 1 0.20 0 0
CUI: C3809233
Disease: NOONAN SYNDROME 8
NOONAN SYNDROME 8 		1 0 1 0.20 0 0