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: C0233697
Disease: Obsessions
Obsessions 		8 5 5 5.2E-02 5 0.31
CUI: C0236000
Disease: Jaw pain
Jaw pain 		6 1 1 1.0E-02 1 6.2E-02
CUI: C1335168
Disease: Ovarian mucinous tumor
Ovarian mucinous tumor 		11 1 2 1.9E-02 1 6.2E-02
CUI: C1389280
Disease: Basal ganglia calcification
Basal ganglia calcification 		22 3 1 8.7E-03 1 5.6E-02
CUI: C4023353
Disease: Abnormality of coordination
Abnormality of coordination 		2 3 1 1.1E-02 1 5.6E-02
CUI: C1859846
Disease: Childhood-onset truncal obesity
Childhood-onset truncal obesity 		11 4 4 4.0E-02 1 5.3E-02
CUI: C2751642
Disease: GLIOMA SUSCEPTIBILITY 2
GLIOMA SUSCEPTIBILITY 2 		1 6 1 1.1E-02 1 4.8E-02
CUI: C0796208
Disease: MENTAL RETARDATION, X-LINKED 3
MENTAL RETARDATION, X-LINKED 3 		3 7 1 1.0E-02 1 4.5E-02
CUI: C1848599
Disease: VACTERL Association With Hydrocephalus
VACTERL Association With Hydrocephalus 		5 7 1 1.0E-02 1 4.5E-02
CUI: C2673700
Disease: Brisk reflexes
Brisk reflexes 		31 7 2 1.6E-02 1 4.5E-02
CUI: C4018849
Disease: Abnormal fear/anxiety-related behavior
Abnormal fear/anxiety-related behavior 		5 7 2 2.1E-02 1 4.5E-02
CUI: C0018552
Disease: Hamartoma
Hamartoma 		91 8 1 5.4E-03 1 4.3E-02
CUI: C4014821
Disease: Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome 		1 12 1 1.1E-02 1 3.7E-02
CUI: C1836923
Disease: Gastrointestinal dysmotility
Gastrointestinal dysmotility 		28 13 1 8.3E-03 1 3.6E-02
CUI: C4012968
Disease: Mild global developmental delay
Mild global developmental delay 		36 13 2 1.6E-02 1 3.6E-02
CUI: C0027497
Disease: Nausea
Nausea 		161 14 10 4.1E-02 1 3.4E-02
CUI: C0239998
Disease: Recurrent infections
Recurrent infections 		127 14 7 3.3E-02 1 3.4E-02
CUI: C0334533
Disease: Arteriovenous hemangioma
Arteriovenous hemangioma 		76 14 4 2.4E-02 1 3.4E-02
CUI: C3489733
Disease: Oculomotor apraxia
Oculomotor apraxia 		92 14 4 2.2E-02 1 3.4E-02
CUI: C3551915
Disease: MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO
MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO 		5 16 1 1.0E-02 1 3.2E-02
CUI: C0040137
Disease: Thyroid Nodule
Thyroid Nodule 		150 17 2 8.3E-03 1 3.1E-02
CUI: C4693860
Disease: DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES
DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES 		2 17 2 2.1E-02 1 3.1E-02
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities 		355 19 17 3.9E-02 1 2.9E-02
CUI: C2063866
Disease: Depressive Disorder, Treatment-Resistant
Depressive Disorder, Treatment-Resistant 		66 19 5 3.2E-02 1 2.9E-02
CUI: C0008489
Disease: Chorea
Chorea 		168 20 8 3.1E-02 1 2.9E-02