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: C0150988
Disease: Sclerodactyly
Sclerodactyly
0 1 0 0 1 0.12
CORONARY ARTERY DISEASE, MODIFIER OF
0 1 0 0 1 0.12
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
0 1 0 0 1 0.12
CUI: C2677079
Disease: Inflammatory Bowel Disease 19
Inflammatory Bowel Disease 19
0 1 0 0 1 0.12
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO
0 1 0 0 1 0.12
CUI: C0005890
Disease: Body Height
Body Height
1903 0 1 5.2E-04 0 0
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
2165 0 2 9.1E-04 0 0
CUI: C1384666
Disease: hearing impairment
hearing impairment
740 0 1 1.3E-03 0 0
CUI: C0033377
Disease: Ptosis
Ptosis
607 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: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
590 0 1 1.6E-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: C0019209
Disease: Hepatomegaly
Hepatomegaly
523 0 1 1.8E-03 0 0
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
507 0 1 1.9E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 1.9E-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: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
433 0 1 2.2E-03 0 0
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability
429 0 1 2.2E-03 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
429 0 1 2.2E-03 0 0
CUI: C1836542
Disease: Depressed nasal bridge
Depressed nasal bridge
426 0 1 2.2E-03 0 0
CUI: C3665347
Disease: Visual Impairment
Visual Impairment
422 0 1 2.2E-03 0 0