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: C0033246
Disease: Proctitis
Proctitis
0 2 0 0 1 7.7E-02
CUI: C0233689
Disease: Delusion of infidelity
Delusion of infidelity
0 1 0 0 1 8.3E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 5.0E-02
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
0 15 0 0 1 3.8E-02
SPINOCEREBELLAR ATAXIA WITH EPILEPSY
0 2 0 0 1 7.7E-02
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
0 5 0 0 1 6.2E-02
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome
0 1 0 0 1 8.3E-02
CUI: C3683791
Disease: Ataxia Neuropathy Spectrum
Ataxia Neuropathy Spectrum
0 2 0 0 1 7.7E-02
CUI: C3888962
Disease: POLG mutation
POLG mutation
0 7 0 0 1 5.6E-02
CUI: C1861403
Disease: Variable expressivity
Variable expressivity
319 0 1 2.4E-03 0 0
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
272 0 1 2.7E-03 0 0
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
269 0 1 2.8E-03 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
255 0 1 2.9E-03 0 0
CUI: C0153594
Disease: Malignant neoplasm of testis
Malignant neoplasm of testis
253 0 1 2.9E-03 0 0
CUI: C3888194
Disease: MIXED LINEAGE LEUKEMIA
MIXED LINEAGE LEUKEMIA
240 0 1 3.0E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 3.0E-03 0 0
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
234 0 1 3.0E-03 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus
213 0 1 3.3E-03 0 0
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase
212 0 1 3.3E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
209 0 1 3.3E-03 0 0
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
197 0 1 3.4E-03 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features
194 0 1 3.5E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 0 1 3.5E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly
186 0 1 3.6E-03 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia
184 0 1 3.6E-03 0 0