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: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 3.7E-02
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 2 7.4E-02
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 3.8E-02
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 3.8E-02
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0 141 0 0 1 6.0E-03
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0 132 0 0 1 6.4E-03
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		249 0 1 1.4E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 1.6E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 1.6E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 1 1.6E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria 		127 0 1 1.7E-03 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia 		118 0 1 1.7E-03 0 0
CUI: C0431447
Disease: Synophrys
Synophrys 		111 0 1 1.7E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 1 1.8E-03 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia 		100 0 1 1.8E-03 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation 		98 0 1 1.8E-03 0 0
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		96 0 1 1.8E-03 0 0
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear 		95 0 1 1.8E-03 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers 		92 0 1 1.8E-03 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 1.8E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 1.8E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.8E-03 0 0
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		82 142 1 1.8E-03 1 6.0E-03
CUI: C0241240
Disease: Tall stature
Tall stature 		79 0 1 1.9E-03 0 0
CUI: C0424731
Disease: Single transverse palmar crease
Single transverse palmar crease 		78 0 1 1.9E-03 0 0