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: C0154038
Disease: Benign neoplasm of thyroid gland
Benign neoplasm of thyroid gland
0 4 0 0 1 4.8E-02
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder
0 59 0 0 1 1.3E-02
Intestinal metaplasia of gastric mucosa
0 1 0 0 1 5.6E-02
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F
0 31 0 0 1 2.1E-02
Multi vessel coronary artery disease
0 1 0 0 1 5.6E-02
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 1 1.4E-03 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism
586 0 1 1.4E-03 0 0
Delayed speech and language development
560 0 1 1.5E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 1.7E-03 0 0
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
439 0 1 1.8E-03 0 0
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding)
427 0 1 1.9E-03 0 0
CUI: C3665347
Disease: Visual Impairment
Visual Impairment
422 0 1 1.9E-03 0 0
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly
410 0 1 1.9E-03 0 0
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
399 0 1 2.0E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability
854 0 2 2.1E-03 0 0
CUI: C0221355
Disease: Macrocephaly
Macrocephaly
367 0 1 2.1E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
312 0 1 2.4E-03 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy
306 0 1 2.4E-03 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy
305 0 1 2.4E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus
716 0 2 2.4E-03 0 0
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger
284 0 1 2.5E-03 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
272 0 1 2.6E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 2.6E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus
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