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: C0232474
Disease: Increased peristalsis
Increased peristalsis 		1 0 1 0.50 0 0
CUI: C0265201
Disease: De Sanctis-Cacchione syndrome
De Sanctis-Cacchione syndrome 		1 0 1 0.50 0 0
CUI: C0281967
Disease: Retinal infarction
Retinal infarction 		1 0 1 0.50 0 0
CUI: C0403647
Disease: Hypotonic bladder disorder
Hypotonic bladder disorder 		1 0 1 0.50 0 0
CUI: C0741621
Disease: Brachial artery occlusion
Brachial artery occlusion 		1 0 1 0.50 0 0
CUI: C1303010
Disease: Mydriasis, Congenital
Mydriasis, Congenital 		1 0 1 0.50 0 0
CUI: C1851430
Disease: Subcortical white matter calcifications
Subcortical white matter calcifications 		1 0 1 0.50 0 0
CUI: C1851431
Disease: Cerebellar calcifications
Cerebellar calcifications 		1 0 1 0.50 0 0
CUI: C1859224
Disease: Second metatarsal posteriorly placed
Second metatarsal posteriorly placed 		1 0 1 0.50 0 0
CUI: C3151063
Disease: MACULAR DEGENERATION, AGE-RELATED, 5
MACULAR DEGENERATION, AGE-RELATED, 5 		1 5 1 0.50 1 0.14
CUI: C3551173
Disease: UV-SENSITIVE SYNDROME 1
UV-SENSITIVE SYNDROME 1 		1 0 1 0.50 0 0
CUI: C4024826
Disease: Pigmentation anomalies of sun-exposed skin
Pigmentation anomalies of sun-exposed skin 		1 0 1 0.50 0 0
CUI: C4310783
Disease: PREMATURE OVARIAN FAILURE 11
PREMATURE OVARIAN FAILURE 11 		1 0 1 0.50 0 0
CUI: C0158638
Disease: Congenital anomaly of cerebrovascular system
Congenital anomaly of cerebrovascular system 		2 0 1 0.33 0 0
CUI: C0392775
Disease: Cystic medial necrosis of aorta
Cystic medial necrosis of aorta 		2 0 1 0.33 0 0
CUI: C0751037
Disease: Cockayne Syndrome, Type III
Cockayne Syndrome, Type III 		2 0 1 0.33 0 0
CUI: C1846837
Disease: Aortic Aneurysm, Familial Thoracic 2
Aortic Aneurysm, Familial Thoracic 2 		2 0 1 0.33 0 0
CUI: C1857638
Disease: Patchy demyelination of subcortical white matter
Patchy demyelination of subcortical white matter 		2 0 1 0.33 0 0
CUI: C1859223
Disease: Deep longitudinal plantar crease
Deep longitudinal plantar crease 		2 0 1 0.33 0 0
CUI: C4025648
Disease: Abnormal peripheral myelination
Abnormal peripheral myelination 		2 0 1 0.33 0 0
CUI: C4289994
Disease: Adenosine Deaminase 2 Deficiency
Adenosine Deaminase 2 Deficiency 		2 0 1 0.33 0 0
CUI: C4477072
Disease: Iris flocculi
Iris flocculi 		2 0 1 0.33 0 0
CUI: C0239761
Disease: Gonadal hypoplasia
Gonadal hypoplasia 		3 0 1 0.25 0 0
CUI: C1857651
Disease: Ivory epiphyses of the phalanges of the hand
Ivory epiphyses of the phalanges of the hand 		3 0 1 0.25 0 0
CUI: C2242574
Disease: Compulsive sexual behaviour
Compulsive sexual behaviour 		3 0 1 0.25 0 0