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: C0158538
Disease: Other congenital anomalies of nervous system
Other congenital anomalies of nervous system 		1 0 1 3.3E-02 0 0
CUI: C0232874
Disease: Febrile proteinuria
Febrile proteinuria 		1 0 1 3.3E-02 0 0
CUI: C0349711
Disease: Sialic storage disease
Sialic storage disease 		1 0 1 3.3E-02 0 0
CUI: C0431379
Disease: Laminar heterotopia
Laminar heterotopia 		1 0 1 3.3E-02 0 0
CUI: C0796124
Disease: Proud Syndrome
Proud Syndrome 		1 0 1 3.3E-02 0 0
CUI: C0849668
Disease: peri-menopausal
peri-menopausal 		1 0 1 3.3E-02 0 0
CUI: C1622439
Disease: Lentiglobus
Lentiglobus 		1 0 1 3.3E-02 0 0
CUI: C1838239
Disease: Band Heterotopia of Brain
Band Heterotopia of Brain 		1 0 1 3.3E-02 0 0
CUI: C1843003
Disease: MITRAL VALVE PROLAPSE, MYXOMATOUS 2
MITRAL VALVE PROLAPSE, MYXOMATOUS 2 		1 0 1 3.3E-02 0 0
CUI: C1846171
Disease: Lissencephaly, X-Linked, 2
Lissencephaly, X-Linked, 2 		1 0 1 3.3E-02 0 0
CUI: C1846172
Disease: Hydranencephaly and Abnormal Genitalia
Hydranencephaly and Abnormal Genitalia 		1 0 1 3.3E-02 0 0
CUI: C1848070
Disease: Lissencephaly and agenesis of corpus callosum
Lissencephaly and agenesis of corpus callosum 		1 0 1 3.3E-02 0 0
CUI: C1963905
Disease: Infantile free sialic acid storage disease
Infantile free sialic acid storage disease 		1 0 1 3.3E-02 0 0
CUI: C2713392
Disease: Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency
Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency 		1 0 1 3.3E-02 0 0
CUI: C2750247
Disease: Polymicrogyria, Asymmetric
Polymicrogyria, Asymmetric 		1 0 1 3.3E-02 0 0
CUI: C2880120
Disease: Echovirus enteritis
Echovirus enteritis 		1 0 1 3.3E-02 0 0
CUI: C2931872
Disease: Free sialic acid storage disease
Free sialic acid storage disease 		1 0 1 3.3E-02 0 0
CUI: C3809875
Disease: VAN MALDERGEM SYNDROME 2
VAN MALDERGEM SYNDROME 2 		1 0 1 3.3E-02 0 0
CUI: C3825592
Disease: Thromboembolism in children
Thromboembolism in children 		1 0 1 3.3E-02 0 0
CUI: C4014939
Disease: HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2
HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2 		1 0 1 3.3E-02 0 0
CUI: C4016431
Disease: CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH QUADRUPEDAL LOCOMOTION 1
CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH QUADRUPEDAL LOCOMOTION 1 		1 0 1 3.3E-02 0 0
CUI: C4022041
Disease: Hypoammonemia
Hypoammonemia 		1 0 1 3.3E-02 0 0
CUI: C4024767
Disease: Dense posterior cortical cataract
Dense posterior cortical cataract 		1 0 1 3.3E-02 0 0
CUI: C4305529
Disease: Dent disease type 2
Dent disease type 2 		1 0 1 3.3E-02 0 0
CUI: C4551950
Disease: VAN MALDERGEM SYNDROME 1
VAN MALDERGEM SYNDROME 1 		1 0 1 3.3E-02 0 0