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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 2.8E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.8E-03
CUI: C1095928
Disease: Secondary hyperthyroidism
Secondary hyperthyroidism 		0 1 0 0 1 2.8E-03
CUI: C1299432
Disease: Multi vessel coronary artery disease
Multi vessel coronary artery disease 		0 1 0 0 1 2.8E-03
CUI: C1318233
Disease: immunoglobulin G index
immunoglobulin G index 		0 4 0 0 1 2.8E-03
CUI: C1446147
Disease: IgG Index (procedure)
IgG Index (procedure) 		0 4 0 0 1 2.8E-03
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 2.8E-03
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 2.8E-03
CUI: C1868512
Disease: Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 		0 2 0 0 1 2.8E-03
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		0 46 0 0 3 7.6E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.8E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.8E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 2.8E-03
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 1.3E-03 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		106 0 1 1.4E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 1.5E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 1 1.5E-03 0 0
CUI: C4551488
Disease: Bifid uvula
Bifid uvula 		97 0 1 1.5E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 1.5E-03 0 0
CUI: C0566620
Disease: Nasal voice
Nasal voice 		93 0 1 1.5E-03 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers 		92 0 1 1.5E-03 0 0
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		90 0 1 1.5E-03 0 0
CUI: C0003119
Disease: Anophthalmos
Anophthalmos 		89 0 1 1.5E-03 0 0
CUI: C1837463
Disease: Narrow face
Narrow face 		87 0 1 1.5E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 1.5E-03 0 0