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: C1853238
Disease: Conotruncal defect
Conotruncal defect
51 0 1 1.9E-02 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis
55 0 1 1.7E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 1 1.6E-02 0 0
Childhood Ataxia with Central Nervous System Hypomyelinization
59 0 1 1.6E-02 0 0
CUI: C0030232
Disease: Pallor
Pallor
124 0 2 1.6E-02 0 0
CUI: C0917996
Disease: Cerebral Aneurysm
Cerebral Aneurysm
65 0 1 1.5E-02 0 0
CUI: C0016412
Disease: Folic Acid Deficiency
Folic Acid Deficiency
70 0 1 1.4E-02 0 0
CUI: C1737329
Disease: Dysmorphism
Dysmorphism
80 0 1 1.2E-02 0 0
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
83 0 1 1.2E-02 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis
85 0 1 1.1E-02 0 0
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
85 0 1 1.1E-02 0 0
CUI: C4021813
Disease: Oral cleft
Oral cleft
85 0 1 1.1E-02 0 0
CUI: C0013221
Disease: Drug toxicity
Drug toxicity
86 0 1 1.1E-02 0 0
CUI: C0041755
Disease: Adverse reaction to drug
Adverse reaction to drug
87 0 1 1.1E-02 0 0
CUI: C2931384
Disease: Moyamoya disease 1
Moyamoya disease 1
92 0 1 1.1E-02 0 0
CUI: C0042963
Disease: Vomiting
Vomiting
303 0 3 9.9E-03 0 0
Cleft Lip with or without Cleft Palate
99 0 1 9.8E-03 0 0
CUI: C1142533
Disease: Smooth philtrum
Smooth philtrum
105 0 1 9.3E-03 0 0
CUI: C1962966
Disease: Retinopathy, CTCAE
Retinopathy, CTCAE
108 0 1 9.0E-03 0 0
CUI: C0038362
Disease: Stomatitis
Stomatitis
109 0 1 8.9E-03 0 0
CUI: C0011206
Disease: Delirium
Delirium
110 0 1 8.8E-03 0 0
CUI: C0019061
Disease: Hemolytic-Uremic Syndrome
Hemolytic-Uremic Syndrome
110 0 1 8.8E-03 0 0
CUI: C0234133
Disease: Extrapyramidal sign
Extrapyramidal sign
116 0 1 8.4E-03 0 0
CUI: C0024291
Disease: Lymphohistiocytosis, Hemophagocytic
Lymphohistiocytosis, Hemophagocytic
117 0 1 8.3E-03 0 0
CUI: C0026654
Disease: Moyamoya Disease
Moyamoya Disease
117 0 1 8.3E-03 0 0