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: C1851504
Disease: Aortic aneurysm, familial thoracic 4
Aortic aneurysm, familial thoracic 4 		2 0 2 0.67 0 0
CUI: C1336007
Disease: Small Intestinal Sarcoma
Small Intestinal Sarcoma 		1 0 1 0.33 0 0
CUI: C1857977
Disease: MICROHYDRANENCEPHALY
MICROHYDRANENCEPHALY 		1 0 1 0.33 0 0
CUI: C2062501
Disease: acute myelomonoblastic leukemia
acute myelomonoblastic leukemia 		1 0 1 0.33 0 0
CUI: C3151461
Disease: LISSENCEPHALY 4
LISSENCEPHALY 4 		1 0 1 0.33 0 0
CUI: C3809288
Disease: LEFT VENTRICULAR NONCOMPACTION 8
LEFT VENTRICULAR NONCOMPACTION 8 		1 0 1 0.33 0 0
CUI: C3809289
Disease: CARDIOMYOPATHY, DILATED, 1LL
CARDIOMYOPATHY, DILATED, 1LL 		1 0 1 0.33 0 0
CUI: C4023757
Disease: Abnormal dura mater morphology
Abnormal dura mater morphology 		1 0 1 0.33 0 0
CUI: C4476560
Disease: Thalamic edema
Thalamic edema 		1 0 1 0.33 0 0
CUI: C4476589
Disease: Dysgenesis of the thalamus
Dysgenesis of the thalamus 		1 0 1 0.33 0 0
CUI: C4551473
Disease: Cystic medial necrosis
Cystic medial necrosis 		1 0 1 0.33 0 0
CUI: C0392775
Disease: Cystic medial necrosis of aorta
Cystic medial necrosis of aorta 		2 0 1 0.25 0 0
CUI: C0740385
Disease: Aneurysm, Middle Cerebral Artery
Aneurysm, Middle Cerebral Artery 		2 0 1 0.25 0 0
CUI: C1834387
Disease: Abnormal iris pigmentation
Abnormal iris pigmentation 		2 0 1 0.25 0 0
CUI: C1837247
Disease: Antenatal intracerebral hemorrhage
Antenatal intracerebral hemorrhage 		2 0 1 0.25 0 0
CUI: C1332156
Disease: Acute myelomonocytic leukemia with abnormal eosinophils
Acute myelomonocytic leukemia with abnormal eosinophils 		3 0 1 0.20 0 0
CUI: C4020755
Disease: Abnormality of fontanelles
Abnormality of fontanelles 		3 0 1 0.20 0 0
CUI: C4021520
Disease: Abnormal cerebral artery morphology
Abnormal cerebral artery morphology 		3 0 1 0.20 0 0
CUI: C1533174
Disease: Acute myeloid leukemia, inv(16)(p13q22)
Acute myeloid leukemia, inv(16)(p13q22) 		4 0 1 0.17 0 0
CUI: C0151315
Disease: Neck stiffness
Neck stiffness 		5 0 1 0.14 0 0
CUI: C0265490
Disease: Trisomy 22
Trisomy 22 		5 0 1 0.14 0 0
CUI: C4023607
Disease: Abnormal corpus striatum morphology
Abnormal corpus striatum morphology 		5 0 1 0.14 0 0
CUI: C0232475
Disease: Decreased peristalsis
Decreased peristalsis 		6 0 1 0.12 0 0
CUI: C1842870
Disease: Chromosome 1p36 Deletion Syndrome
Chromosome 1p36 Deletion Syndrome 		6 0 1 0.12 0 0
CUI: C4476545
Disease: Dilatation of the ventricular cavity
Dilatation of the ventricular cavity 		6 0 1 0.12 0 0