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 3.2E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.2E-03
CUI: C0201952
Disease: Chloride measurement
Chloride measurement 		0 19 0 0 1 3.1E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.2E-03
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 3.2E-03
CUI: C0557163
Disease: Household income
Household income 		0 2 0 0 1 3.2E-03
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 3.2E-03
CUI: C1843898
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 (disorder)
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 (disorder) 		0 1 0 0 1 3.2E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 3.2E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 3.2E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.2E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 3.2E-03
CUI: C4546209
Disease: Chronic pain following trauma
Chronic pain following trauma 		0 1 0 0 1 3.2E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 3.2E-03
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia 		118 0 1 1.4E-03 0 0
CUI: C0025995
Disease: Micromelia
Micromelia 		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: C0376480
Disease: Gingival Overgrowth
Gingival Overgrowth 		100 0 1 1.5E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc 		98 0 1 1.5E-03 0 0
CUI: C4025814
Disease: Abnormality of the metaphysis
Abnormality of the metaphysis 		97 0 1 1.5E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 1.5E-03 0 0
CUI: C0878659
Disease: Disproportionate short stature
Disproportionate short stature 		86 0 1 1.5E-03 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology 		86 0 1 1.5E-03 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 0 1 1.5E-03 0 0
CUI: C1853241
Disease: Flat face
Flat face 		83 0 1 1.5E-03 0 0