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: C1717804
Disease: Emphysema or COPD
Emphysema or COPD 		3 0 2 0.33 0 0
CUI: C0340613
Disease: Arterial aneurysm
Arterial aneurysm 		10 0 3 0.25 0 0
CUI: C0334083
Disease: Connective tissue nevus, NOS
Connective tissue nevus, NOS 		6 0 2 0.22 0 0
CUI: C1862932
Disease: ANEURYSM, INTRACRANIAL BERRY, 1 (disorder)
ANEURYSM, INTRACRANIAL BERRY, 1 (disorder) 		6 0 2 0.22 0 0
CUI: C0042140
Disease: Uterine Prolapse
Uterine Prolapse 		12 0 3 0.21 0 0
CUI: C0006542
Disease: Byssinosis
Byssinosis 		1 0 1 0.20 0 0
CUI: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 0.20 0 0
CUI: C0030328
Disease: Panniculitis, Nodular Nonsuppurative
Panniculitis, Nodular Nonsuppurative 		1 0 1 0.20 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 0.20 0 0
CUI: C0241876
Disease: Obstructive emphysema
Obstructive emphysema 		1 0 1 0.20 0 0
CUI: C0266284
Disease: Lingual Thyroid
Lingual Thyroid 		1 0 1 0.20 0 0
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV 		7 0 2 0.20 0 0
CUI: C0334689
Disease: C cell tumor
C cell tumor 		1 0 1 0.20 0 0
CUI: C0340649
Disease: Dissection of iliac artery
Dissection of iliac artery 		1 0 1 0.20 0 0
CUI: C0343972
Disease: Schistosomal splenomegaly
Schistosomal splenomegaly 		1 0 1 0.20 0 0
CUI: C0406584
Disease: Acrogeria, gottron type
Acrogeria, gottron type 		1 0 1 0.20 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 0.20 0 0
CUI: C0743188
Disease: diarrhea persistent
diarrhea persistent 		1 0 1 0.20 0 0
CUI: C1262008
Disease: Hyperphosphatasemia
Hyperphosphatasemia 		1 0 1 0.20 0 0
CUI: C1266055
Disease: Mixed medullary-follicular carcinoma
Mixed medullary-follicular carcinoma 		1 0 1 0.20 0 0
CUI: C1266099
Disease: Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation
Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation 		1 0 1 0.20 0 0
CUI: C1275239
Disease: Dermatomyofibroma
Dermatomyofibroma 		1 0 1 0.20 0 0
CUI: C1305147
Disease: Congenital supravalvular aortic stenosis
Congenital supravalvular aortic stenosis 		1 0 1 0.20 0 0
CUI: C1390214
Disease: Internal hemorrhage
Internal hemorrhage 		1 0 1 0.20 0 0
CUI: C1394142
Disease: Cortical hyperostosis
Cortical hyperostosis 		1 0 1 0.20 0 0