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: C0339619
Disease: Congenital esotropia
Congenital esotropia
0 2 0 0 1 1.0E-01
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.7E-03 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE
477 0 1 1.9E-03 0 0
CUI: C0013421
Disease: Dystonia
Dystonia
453 0 1 2.0E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
433 0 1 2.0E-03 0 0
CUI: C0042834
Disease: Vital capacity
Vital capacity
430 0 1 2.0E-03 0 0
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability
429 0 1 2.0E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum
385 0 1 2.3E-03 0 0
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
1156 0 3 2.5E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 5 2.6E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 1 2.6E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence
645 0 2 2.8E-03 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
285 0 1 2.9E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
272 0 1 3.0E-03 0 0
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
269 0 1 3.0E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus
265 0 1 3.1E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 3.1E-03 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
255 0 1 3.2E-03 0 0
CUI: C0004509
Disease: Azoospermia
Azoospermia
254 0 1 3.2E-03 0 0
CUI: C0030312
Disease: Pancytopenia
Pancytopenia
253 0 1 3.2E-03 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
251 0 1 3.2E-03 0 0
Delayed speech and language development
560 0 2 3.2E-03 0 0
CUI: C0489786
Disease: Height
Height
249 0 1 3.2E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability
854 0 3 3.3E-03 0 0
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome
234 0 1 3.4E-03 0 0