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: C0264411
Disease: Hay fever with asthma
Hay fever with asthma
0 1 0 0 1 3.2E-02
CUI: C0393761
Disease: Middle insomnia
Middle insomnia
0 1 0 0 1 3.2E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 2.6E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
272 0 1 1.9E-03 0 0
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
234 0 1 2.1E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
216 0 1 2.2E-03 0 0
CUI: C0005612
Disease: Birth Weight
Birth Weight
214 0 1 2.2E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 2.2E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
190 0 1 2.3E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum
182 0 1 2.3E-03 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers
171 0 1 2.4E-03 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
160 0 1 2.5E-03 0 0
CUI: C1837260
Disease: Prominent forehead
Prominent forehead
159 0 1 2.5E-03 0 0
CUI: C0221358
Disease: Long narrow head
Long narrow head
154 0 1 2.5E-03 0 0
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
144 0 1 2.6E-03 0 0
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
143 0 1 2.6E-03 0 0
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
139 0 1 2.6E-03 0 0
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
139 0 1 2.6E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior
135 0 1 2.6E-03 0 0
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
135 0 1 2.6E-03 0 0
Platelet Component Distribution Width Measurement
134 0 1 2.6E-03 0 0
CUI: C0024790
Disease: Paroxysmal nocturnal hemoglobinuria
Paroxysmal nocturnal hemoglobinuria
132 0 1 2.6E-03 0 0
CUI: C0021359
Disease: Infertility
Infertility
130 0 1 2.7E-03 0 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
130 0 1 2.7E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay
130 0 1 2.7E-03 0 0