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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 4.8E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 4.8E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 3.7E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 9.5E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 3 0.13
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 4.3E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 4.8E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 9.1E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 9.1E-04 0 0
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		57 0 1 9.1E-04 0 0
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		54 0 1 9.2E-04 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 1 9.2E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 9.2E-04 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 9.2E-04 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 9.3E-04 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 9.3E-04 0 0
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis 		41 0 1 9.3E-04 0 0
CUI: C0029489
Disease: Other alopecia
Other alopecia 		39 0 1 9.3E-04 0 0
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3 		39 0 1 9.3E-04 0 0
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2 		39 0 1 9.3E-04 0 0
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1 		39 0 1 9.3E-04 0 0
CUI: C0342684
Disease: Ocular albinism, type I
Ocular albinism, type I 		38 0 1 9.3E-04 0 0
CUI: C1838681
Disease: Rapidly progressive
Rapidly progressive 		38 0 1 9.3E-04 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular 		37 0 1 9.3E-04 0 0
CUI: C0454651
Disease: Specific language impairment
Specific language impairment 		34 0 1 9.3E-04 0 0