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: C4024945
Disease: Generalized cerebral atrophy/hypoplasia
Generalized cerebral atrophy/hypoplasia 		14 0 1 2.4E-04 0 0
CUI: C0015396
Disease: Eye Color
Eye Color 		13 0 1 2.4E-04 0 0
CUI: C0220787
Disease: Endotracheal aspiration
Endotracheal aspiration 		13 0 1 2.4E-04 0 0
CUI: C0423276
Disease: Shallow anterior chamber of eye
Shallow anterior chamber of eye 		13 0 1 2.4E-04 0 0
CUI: C0700198
Disease: Pulmonary aspiration
Pulmonary aspiration 		13 0 1 2.4E-04 0 0
CUI: C0752202
Disease: Childhood Onset Dystonias
Childhood Onset Dystonias 		13 0 1 2.4E-04 0 0
CUI: C1386091
Disease: Acromicria
Acromicria 		13 0 1 2.4E-04 0 0
CUI: C1399226
Disease: Ectopic rhythm
Ectopic rhythm 		13 0 1 2.4E-04 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		13 0 1 2.4E-04 0 0
CUI: C1963221
Disease: Aspiration, CTCAE
Aspiration, CTCAE 		13 0 1 2.4E-04 0 0
CUI: C2827071
Disease: Unintentional Material Aspiration
Unintentional Material Aspiration 		13 0 1 2.4E-04 0 0
CUI: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
Night Blindness, Congenital Stationary, Type 1A 		13 0 1 2.4E-04 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		13 0 1 2.4E-04 0 0
CUI: C3711543
Disease: X-Linked Csnb
X-Linked Csnb 		13 0 1 2.4E-04 0 0
CUI: C3806510
Disease: Horizontal ribs
Horizontal ribs 		13 0 1 2.4E-04 0 0
CUI: C4022810
Disease: Abnormality of nervous system morphology
Abnormality of nervous system morphology 		13 0 1 2.4E-04 0 0
CUI: C4024610
Disease: Leg muscle stiffness
Leg muscle stiffness 		13 0 1 2.4E-04 0 0
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		13 0 1 2.4E-04 0 0
CUI: C0027412
Disease: Opioid-Related Disorders
Opioid-Related Disorders 		12 0 1 2.4E-04 0 0
CUI: C0027612
Disease: Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital, Hereditary, and Neonatal Diseases and Abnormalities 		12 0 1 2.4E-04 0 0
CUI: C0241775
Disease: Organic aciduria
Organic aciduria 		12 0 1 2.4E-04 0 0
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder 		12 0 1 2.4E-04 0 0
CUI: C0265222
Disease: Royer Syndrome
Royer Syndrome 		12 0 1 2.4E-04 0 0
CUI: C0270912
Disease: Charcot-Marie-Tooth Disease, Type Ib
Charcot-Marie-Tooth Disease, Type Ib 		12 0 1 2.4E-04 0 0
CUI: C0337439
Disease: Iron measurement
Iron measurement 		12 0 1 2.4E-04 0 0