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: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome 		0 3 0 0 1 6.8E-03
CUI: C0018425
Disease: Gyrate Atrophy
Gyrate Atrophy 		0 35 0 0 1 5.6E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 6.8E-03
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia 		0 1 0 0 1 6.8E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 6.8E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 6.6E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 6.8E-03
CUI: C0280252
Disease: stage, colon cancer
stage, colon cancer 		0 2 0 0 1 6.8E-03
CUI: C0373601
Disease: Dihydrotestosterone Assay
Dihydrotestosterone Assay 		0 2 0 0 1 6.8E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 6.8E-03
CUI: C0432209
Disease: Dyssegmental dysplasia, Rolland-Desbuquois type
Dyssegmental dysplasia, Rolland-Desbuquois type 		0 1 0 0 1 6.8E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 6.8E-03
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 1.4E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 6.8E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 6.8E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 6.8E-03
CUI: C4017305
Disease: GYRATE ATROPHY OF CHOROID AND RETINA WITH PYRIDOXINE-RESPONSIVE ORNITHINEMIA
GYRATE ATROPHY OF CHOROID AND RETINA WITH PYRIDOXINE-RESPONSIVE ORNITHINEMIA 		0 2 0 0 1 6.8E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 2.1E-02
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 1.3E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 1.5E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 1.5E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 1.5E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria 		127 0 1 1.6E-03 0 0
CUI: C0426429
Disease: Broad nasal tip
Broad nasal tip 		125 0 1 1.6E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 249 1 1.6E-03 1 2.5E-03