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: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 2.8E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 2.8E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 2.8E-03
CUI: C0814144
Disease: endocrine system cancer
endocrine system cancer
0 1 0 0 1 2.8E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 2 5.7E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 2.8E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 2.8E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 2.8E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 3 8.5E-03
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia
59 0 1 3.2E-04 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy
48 0 1 3.2E-04 0 0
Abnormal mitochondria in muscle tissue
39 0 1 3.2E-04 0 0
Decreased activity of the pyruvate dehydrogenase complex
35 0 1 3.2E-04 0 0
Decreased activity of mitochondrial respiratory chain
34 0 1 3.2E-04 0 0
Focal T2 hyperintense brainstem lesion
33 0 1 3.2E-04 0 0
CUI: C0038663
Disease: Suicide attempt
Suicide attempt
31 0 1 3.2E-04 0 0
CUI: C1843637
Disease: Neck flexor weakness
Neck flexor weakness
30 0 1 3.2E-04 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED
30 0 1 3.2E-04 0 0
Aplasia/Hypoplasia of the cerebellar vermis
30 0 1 3.2E-04 0 0
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
30 0 1 3.2E-04 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL
30 0 1 3.2E-04 0 0
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy
29 0 1 3.2E-04 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
29 0 1 3.2E-04 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL
29 0 1 3.2E-04 0 0
Hereditary Autosomal Dominant Spastic Paraplegia
27 0 1 3.2E-04 0 0