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: C0348426
Disease: Benign neoplasm of meninges
Benign neoplasm of meninges 		1 0 1 1.00 0 0
CUI: C0871976
Disease: facial features
facial features 		1 1 1 1.00 1 3.2E-02
CUI: C4021076
Disease: Iron accumulation in brain
Iron accumulation in brain 		3 38 1 0.33 1 1.5E-02
CUI: C0796184
Disease: Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence
Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence 		4 0 1 0.25 0 0
CUI: C4293686
Disease: Periventricular white matter hyperdensities
Periventricular white matter hyperdensities 		4 1 1 0.25 1 3.2E-02
CUI: C0205671
Disease: Infections, Arenavirus
Infections, Arenavirus 		12 0 1 8.3E-02 0 0
CUI: C1836806
Disease: Mild microcephaly
Mild microcephaly 		12 5 1 8.3E-02 1 2.9E-02
CUI: C1857482
Disease: Slender finger
Slender finger 		20 5 1 5.0E-02 1 2.9E-02
CUI: C4289792
Disease: Chronic Active EBV Infection of T-and NK-Cell Type, Systemic Form
Chronic Active EBV Infection of T-and NK-Cell Type, Systemic Form 		22 0 1 4.5E-02 0 0
CUI: C1266086
Disease: Polymorphous low grade adenocarcinoma
Polymorphous low grade adenocarcinoma 		23 0 1 4.3E-02 0 0
CUI: C0206608
Disease: Flavivirus Infections
Flavivirus Infections 		30 0 1 3.3E-02 0 0
CUI: C0542519
Disease: Congenital absence of kidney
Congenital absence of kidney 		33 3 1 3.0E-02 1 3.0E-02
CUI: C1955906
Disease: Lymphoma, Extranodal NK-T-Cell
Lymphoma, Extranodal NK-T-Cell 		33 0 1 3.0E-02 0 0
CUI: C0281784
Disease: Benign Meningioma
Benign Meningioma 		35 0 1 2.9E-02 0 0
CUI: C0270790
Disease: Quadriparesis
Quadriparesis 		42 5 1 2.4E-02 1 2.9E-02
CUI: C0401149
Disease: Chronic constipation
Chronic constipation 		47 16 1 2.1E-02 1 2.2E-02
CUI: C0019104
Disease: Hemorrhagic Fevers, Viral
Hemorrhagic Fevers, Viral 		57 0 1 1.8E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation 		58 0 1 1.7E-02 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 1 1.5E-02 0 0
CUI: C0694549
Disease: Community acquired pneumonia
Community acquired pneumonia 		75 0 1 1.3E-02 0 0
CUI: C0856863
Disease: Broad-based gait
Broad-based gait 		75 0 1 1.3E-02 0 0
CUI: C0043124
Disease: West Nile Fever
West Nile Fever 		79 0 1 1.3E-02 0 0
CUI: C0236018
Disease: Aura
Aura 		83 0 1 1.2E-02 0 0
CUI: C0751111
Disease: Awakening Epilepsy
Awakening Epilepsy 		83 0 1 1.2E-02 0 0
CUI: C4021813
Disease: Oral cleft
Oral cleft 		85 0 1 1.2E-02 0 0