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: C4021734
Disease: Abnormality of mitochondrial metabolism
Abnormality of mitochondrial metabolism 		21 0 2 3.3E-02 0 0
CUI: C4073241
Disease: Abnormality of nasopharyngeal adenoids
Abnormality of nasopharyngeal adenoids 		1 0 1 2.4E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 2 7.9E-03 0 0
CUI: C4021243
Disease: Abnormality of thalamus morphology
Abnormality of thalamus morphology 		10 0 2 4.1E-02 0 0
CUI: C4025329
Disease: Abnormality of the anus
Abnormality of the anus 		16 0 1 1.8E-02 0 0
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum 		55 0 1 1.1E-02 0 0
CUI: C4025701
Disease: Abnormality of the cerebral cortex
Abnormality of the cerebral cortex 		11 0 2 4.0E-02 0 0
CUI: C4024158
Disease: Abnormality of the columella
Abnormality of the columella 		2 0 1 2.4E-02 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition 		140 0 1 5.6E-03 0 0
CUI: C0281842
Disease: Abnormality of the fallopian tube
Abnormality of the fallopian tube 		22 0 1 1.6E-02 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		75 0 1 8.7E-03 0 0
CUI: C0857379
Disease: Abnormality of the pinna
Abnormality of the pinna 		85 0 1 8.0E-03 0 0
CUI: C4022447
Disease: Abnormality of the tympanic membrane
Abnormality of the tympanic membrane 		1 0 1 2.4E-02 0 0
CUI: C0431371
Disease: Absence of septum pellucidum
Absence of septum pellucidum 		84 0 1 8.1E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 2 8.3E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 72 3 1.1E-02 1 1.4E-02
CUI: C0266260
Disease: Accessory hepatic duct
Accessory hepatic duct 		1 0 1 2.4E-02 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		209 0 34 0.16 0 0
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis 		149 0 1 5.3E-03 0 0
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease 		294 0 2 6.0E-03 0 0
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		766 0 1 1.2E-03 0 0
CUI: C1855020
Disease: Acute necrotizing encephalopathy
Acute necrotizing encephalopathy 		8 0 1 2.1E-02 0 0
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia 		651 0 1 1.4E-03 0 0
CUI: C1970173
Disease: Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of
Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of 		1 0 1 2.4E-02 0 0
CUI: C0431129
Disease: Adamantinous Craniopharyngioma
Adamantinous Craniopharyngioma 		48 0 1 1.1E-02 0 0