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: C0005890
Disease: Body Height
Body Height
1903 0 1 5.2E-04 0 0
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
1156 0 1 8.5E-04 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
955 0 1 1.0E-03 0 0
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
681 0 1 1.4E-03 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 1 1.6E-03 0 0
Red cell distribution width determination
593 0 1 1.6E-03 0 0
RDW - Red blood cell distribution width result
593 0 1 1.6E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
580 0 1 1.7E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
568 0 1 1.7E-03 0 0
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
563 0 1 1.7E-03 0 0
Delayed speech and language development
560 0 1 1.7E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.8E-03 0 0
CUI: C0040822
Disease: Tremor
Tremor
528 0 1 1.8E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 1.9E-03 0 0
Low density lipoprotein cholesterol measurement
483 0 1 2.0E-03 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE
477 0 1 2.0E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
967 0 2 2.0E-03 0 0
CUI: C0013421
Disease: Dystonia
Dystonia
453 0 1 2.1E-03 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
429 0 1 2.2E-03 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
426 0 1 2.2E-03 0 0
CUI: C3665347
Disease: Visual Impairment
Visual Impairment
422 0 1 2.2E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 2 2.2E-03 0 0
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus
417 0 1 2.3E-03 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
850 0 2 2.3E-03 0 0
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly
410 0 1 2.3E-03 0 0