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: C0576979
Disease: Lesion of salivary gland
Lesion of salivary gland
0 1 0 0 1 1.5E-02
CUI: C4302243
Disease: Autoimmune pancreatitis type 1
Autoimmune pancreatitis type 1
0 1 0 0 1 1.5E-02
CUI: C0021704
Disease: Intelligence
Intelligence
645 0 1 1.3E-03 0 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
473 0 1 1.7E-03 0 0
CUI: C1305855
Disease: Body mass index
Body mass index
1014 0 2 1.8E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
433 0 1 1.9E-03 0 0
CUI: C0042834
Disease: Vital capacity
Vital capacity
430 0 1 1.9E-03 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
429 0 1 1.9E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 4 2.0E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum
385 0 1 2.1E-03 0 0
CUI: C1854301
Disease: Motor delay
Motor delay
384 0 1 2.1E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 1 2.4E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
291 0 1 2.5E-03 0 0
Finding of Mean Corpuscular Hemoglobin
653 0 2 2.7E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
272 0 1 2.7E-03 0 0
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
269 0 1 2.7E-03 0 0
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
269 0 1 2.7E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 2.7E-03 0 0
CUI: C1854114
Disease: Short nose
Short nose
265 0 1 2.7E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
264 0 1 2.7E-03 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
255 0 1 2.8E-03 0 0
CUI: C0489786
Disease: Height
Height
249 0 1 2.8E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 2.9E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 2.9E-03 0 0
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos
235 0 1 3.0E-03 0 0