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: C0014394
Disease: Enuresis
Enuresis 		0 3 0 0 1 8.3E-02
CUI: C1836696
Disease: Lower limb hyperreflexia
Lower limb hyperreflexia 		0 6 0 0 1 6.7E-02
CUI: C1844806
Disease: Weight less than 3rd percentile
Weight less than 3rd percentile 		0 27 0 0 1 2.8E-02
CUI: C1844820
Disease: Range of joint movement increased
Range of joint movement increased 		0 46 0 0 1 1.8E-02
CUI: C1853487
Disease: Thick eyebrow
Thick eyebrow 		0 13 0 0 1 4.5E-02
CUI: C1963101
Disease: Encephalopathy, CTCAE 3.0
Encephalopathy, CTCAE 3.0 		0 24 0 0 1 3.0E-02
CUI: C4023077
Disease: EEG with central focal spikes
EEG with central focal spikes 		0 2 0 0 1 9.1E-02
CUI: C4023353
Disease: Abnormality of coordination
Abnormality of coordination 		0 3 0 0 1 8.3E-02
CUI: C4025792
Disease: EEG with irregular generalized spike and wave complexes
EEG with irregular generalized spike and wave complexes 		0 1 0 0 1 1.0E-01
CUI: C4317045
Disease: Gluten intolerance
Gluten intolerance 		0 1 0 0 1 1.0E-01
CUI: C4693362
Disease: EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2
EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2 		0 7 0 0 1 6.2E-02
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 4.5E-03 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		64 0 1 4.5E-03 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls 		22 0 1 5.6E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 6.2E-03 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 0 1 3.4E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 6.1E-03 0 0
CUI: C0001429
Disease: Adenolymphoma
Adenolymphoma 		21 0 1 5.6E-03 0 0
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms 		23 0 1 5.6E-03 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 5.0E-03 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related 		89 0 1 4.1E-03 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		282 0 1 2.3E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia 		17 0 1 5.7E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 4.9E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis 		25 0 1 5.5E-03 0 0