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: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood
0 20 0 0 1 2.9E-02
CUI: C0745031
Disease: homicidal
homicidal
0 2 0 0 1 5.9E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon
0 1 0 0 1 6.2E-02
Frequent episodic tension-type headache
0 1 0 0 1 6.2E-02
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
338 0 1 1.8E-03 0 0
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
272 0 1 2.0E-03 0 0
CUI: C1854114
Disease: Short nose
Short nose
265 0 1 2.1E-03 0 0
CUI: C1853242
Disease: Midface retrusion
Midface retrusion
228 0 1 2.2E-03 0 0
CUI: C0086437
Disease: Joint laxity
Joint laxity
224 0 1 2.3E-03 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex
218 0 1 2.3E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
216 0 1 2.3E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure
216 0 1 2.3E-03 0 0
CUI: C0333068
Disease: Flexion contracture
Flexion contracture
210 0 1 2.3E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
208 0 1 2.4E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry
206 0 1 2.4E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 2.4E-03 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
197 0 1 2.4E-03 0 0
CUI: C0036920
Disease: Sezary Syndrome
Sezary Syndrome
196 0 1 2.4E-03 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features
194 0 1 2.4E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia
191 0 1 2.5E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum
182 0 1 2.5E-03 0 0
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
Juvenile Myelomonocytic Leukemia
179 0 1 2.5E-03 0 0
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear
176 0 1 2.5E-03 0 0
CUI: C0423224
Disease: Sunken eyes
Sunken eyes
171 0 1 2.6E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement
169 0 1 2.6E-03 0 0