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 7.0E-04
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 7.0E-04
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 7.0E-04
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 7.0E-04
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 1 7.0E-04
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
0 5 0 0 1 7.0E-04
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated
0 2 0 0 1 7.0E-04
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 7.0E-04
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 7.0E-04
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 7.0E-04
CUI: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 2.1E-03 0 0
CUI: C1854114
Disease: Short nose
Short nose
265 0 1 2.1E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
216 0 1 2.4E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
190 0 1 2.6E-03 0 0
CUI: C1836047
Disease: Long face
Long face
182 0 1 2.6E-03 0 0
Malformations of Cortical Development, Group II
180 0 1 2.6E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive
172 0 1 2.7E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia
169 0 1 2.7E-03 0 0
Child Development Disorders, Pervasive
168 0 1 2.7E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 2.7E-03 0 0
Flexion contracture of proximal interphalangeal joint
168 0 1 2.7E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression
165 0 1 2.7E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers
160 0 1 2.8E-03 0 0
CUI: C1837260
Disease: Prominent forehead
Prominent forehead
159 0 1 2.8E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 2.8E-03 0 0