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: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia
0 11 0 0 1 2.1E-03
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia
0 1 0 0 1 2.1E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 2.1E-03
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait
0 2 0 0 1 2.1E-03
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
0 2 0 0 1 2.1E-03
CUI: C1262313
Disease: Invasive Fungal Infections
Invasive Fungal Infections
0 5 0 0 1 2.1E-03
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril
407 0 1 1.6E-03 0 0
CUI: C1397307
Disease: Cardiac fibrosis
Cardiac fibrosis
297 0 1 1.9E-03 0 0
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
284 0 1 1.9E-03 0 0
CUI: C1854114
Disease: Short nose
Short nose
265 0 1 2.0E-03 0 0
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
248 0 1 2.1E-03 0 0
CUI: C0014474
Disease: Ependymoma
Ependymoma
244 0 1 2.1E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 2.1E-03 0 0
Creatine phosphokinase serum increased
228 0 1 2.2E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia
226 0 1 2.2E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears
223 0 1 2.2E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
216 0 1 2.2E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
209 0 1 2.3E-03 0 0
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa
202 0 1 2.3E-03 0 0
CUI: C0035344
Disease: Retinopathy of Prematurity
Retinopathy of Prematurity
202 0 1 2.3E-03 0 0
CUI: C0600427
Disease: Cocaine Dependence
Cocaine Dependence
199 0 1 2.3E-03 0 0
Abnormality of cardiovascular system morphology
198 0 1 2.3E-03 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
197 0 1 2.3E-03 0 0
CUI: C0036920
Disease: Sezary Syndrome
Sezary Syndrome
196 0 1 2.3E-03 0 0
CUI: C0016667
Disease: Fragile X Syndrome
Fragile X Syndrome
194 0 1 2.3E-03 0 0