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 7.2E-03
CUI: C0154038
Disease: Benign neoplasm of thyroid gland
Benign neoplasm of thyroid gland
0 4 0 0 1 7.0E-03
CUI: C0236048
Disease: Polyposis, Gastric
Polyposis, Gastric
0 4 0 0 1 7.0E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 6.9E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 7.2E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 1 7.1E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia
0 1 0 0 1 7.2E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 7.2E-03
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 6.8E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 7.2E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 7.2E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 7.1E-03
CUI: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection
0 2 0 0 1 7.1E-03
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation
340 0 1 1.3E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 1.5E-03 0 0
CUI: C0239676
Disease: High forehead
High forehead
211 0 1 1.5E-03 0 0
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion
211 0 1 1.5E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
208 0 1 1.5E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech
208 0 1 1.5E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 1.6E-03 0 0
Abnormality of cardiovascular system morphology
198 0 1 1.6E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum
182 0 1 1.6E-03 0 0
CUI: C0423224
Disease: Sunken eyes
Sunken eyes
171 0 1 1.6E-03 0 0
Flexion contracture of proximal interphalangeal joint
168 0 1 1.6E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 1.7E-03 0 0