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: C0040046
Disease: Thrombophlebitis
Thrombophlebitis
3 0 2 0.12 0 0
CUI: C0006281
Disease: Congenital bronchogenic cyst
Congenital bronchogenic cyst
4 0 2 0.12 0 0
CUI: C1403996
Disease: Squamous cell metaplasia
Squamous cell metaplasia
4 0 2 0.12 0 0
CUI: C1863411
Disease: Retinal hamartoma
Retinal hamartoma
4 0 2 0.12 0 0
CUI: C1866398
Disease: Proteus-Like Syndrome (disorder)
Proteus-Like Syndrome (disorder)
4 0 2 0.12 0 0
CUI: C1859896
Disease: Progressive macrocephaly
Progressive macrocephaly
5 0 2 0.11 0 0
MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO
5 0 2 0.11 0 0
CUI: C1333989
Disease: Familial meningioma
Familial meningioma
6 0 2 0.11 0 0
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
PTEN Hamartoma Tumor Syndrome
17 0 3 0.10 0 0
CUI: C4021563
Disease: Retinal nonattachment
Retinal nonattachment
7 0 2 1.0E-01 0 0
CUI: C4021567
Disease: Central heterochromia
Central heterochromia
7 0 2 1.0E-01 0 0
CUI: C0334584
Disease: Spongioblastoma
Spongioblastoma
8 0 2 9.5E-02 0 0
CUI: C4025896
Disease: Abnormality of the penis
Abnormality of the penis
8 0 2 9.5E-02 0 0
Cerebral Primitive Neuroectodermal Tumor
9 0 2 9.1E-02 0 0
Abnormal subcutaneous fat tissue distribution
9 0 2 9.1E-02 0 0
CUI: C2931352
Disease: Familial renal cell carcinoma
Familial renal cell carcinoma
9 0 2 9.1E-02 0 0
CUI: C4022024
Disease: Upper limb asymmetry
Upper limb asymmetry
9 0 2 9.1E-02 0 0
CUI: C0205822
Disease: Hibernoma
Hibernoma
10 0 2 8.7E-02 0 0
CUI: C0265552
Disease: Congenital macrodactylia
Congenital macrodactylia
10 0 2 8.7E-02 0 0
CUI: C0334102
Disease: Lymphangiomatosis
Lymphangiomatosis
10 0 2 8.7E-02 0 0
CUI: C0851409
Disease: Glaucoma and ocular hypertension
Glaucoma and ocular hypertension
10 0 2 8.7E-02 0 0
CUI: C1403035
Disease: Subcutaneous lipoma
Subcutaneous lipoma
10 0 2 8.7E-02 0 0
CUI: C1863351
Disease: Calvarial hyperostosis
Calvarial hyperostosis
10 0 2 8.7E-02 0 0
CUI: C3714976
Disease: ACTIVATED PI3K-DELTA SYNDROME
ACTIVATED PI3K-DELTA SYNDROME
10 0 2 8.7E-02 0 0
CUI: C4021744
Disease: Abnormality of the wrist
Abnormality of the wrist
10 0 2 8.7E-02 0 0