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: C3150803
Disease: NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA
NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA 		2 9 2 0.33 2 3.3E-02
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		12 153 4 0.29 23 0.13
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis 		3 7 2 0.29 1 1.7E-02
CUI: C3854181
Disease: Nevus sebaceous
Nevus sebaceous 		3 4 2 0.29 1 1.8E-02
CUI: C4552097
Disease: Nevus Sebaceus of Jadassohn
Nevus Sebaceus of Jadassohn 		3 7 2 0.29 1 1.7E-02
CUI: C0334583
Disease: Pilocytic Astrocytoma
Pilocytic Astrocytoma 		4 0 2 0.25 0 0
CUI: C0206729
Disease: Neurofibrosarcoma
Neurofibrosarcoma 		5 0 2 0.22 0 0
CUI: C1858969
Disease: Decreased lymphocyte apoptosis
Decreased lymphocyte apoptosis 		5 0 2 0.22 0 0
CUI: C1864795
Disease: Superior pectus carinatum
Superior pectus carinatum 		5 0 2 0.22 0 0
CUI: C1864796
Disease: Pectus excavatum of inferior sternum
Pectus excavatum of inferior sternum 		5 0 2 0.22 0 0
CUI: C2674723
Disease: RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER 		5 14 2 0.22 3 4.7E-02
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1 		11 73 3 0.21 21 0.20
CUI: C1860991
Disease: NOONAN SYNDROME 3
NOONAN SYNDROME 3 		6 32 2 0.20 9 0.12
CUI: C2674738
Disease: Abnormality of toe
Abnormality of toe 		6 0 2 0.20 0 0
CUI: C4022025
Disease: Asymmetric growth
Asymmetric growth 		6 0 2 0.20 0 0
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders 		7 0 2 0.18 0 0
CUI: C2674737
Disease: Abnormality of finger
Abnormality of finger 		7 0 2 0.18 0 0
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		1 1 1 0.17 1 1.9E-02
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1 		1 764 1 0.17 20 2.5E-02
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 1 1 0.17 1 1.9E-02
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 3 1 0.17 3 5.7E-02
CUI: C0206728
Disease: Plexiform Neurofibroma
Plexiform Neurofibroma 		1 0 1 0.17 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 1 1 0.17 1 1.9E-02
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 0.17 0 0
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
NEVUS, EPIDERMAL (disorder) 		8 17 2 0.17 2 2.9E-02