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: C0020875
Disease: Ileal Diseases
Ileal Diseases
0 7 0 0 1 3.3E-02
CUI: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood
0 20 0 0 1 2.3E-02
CUI: C0234253
Disease: Rest pain
Rest pain
0 1 0 0 1 4.2E-02
CUI: C0234512
Disease: Prosopagnosia
Prosopagnosia
0 2 0 0 1 4.0E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon
0 1 0 0 1 4.2E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 3.1E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse
0 1 0 0 1 4.2E-02
Frequent episodic tension-type headache
0 1 0 0 1 4.2E-02
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus
417 0 1 2.1E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum
385 0 1 2.2E-03 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression
333 0 1 2.5E-03 0 0
CUI: C0221354
Disease: Frontal bossing
Frontal bossing
321 0 1 2.6E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 1 2.6E-03 0 0
CUI: C3806482
Disease: Recurrent respiratory infections
Recurrent respiratory infections
318 0 1 2.6E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
312 0 1 2.6E-03 0 0
CUI: C0575081
Disease: Gait abnormality
Gait abnormality
312 0 1 2.6E-03 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy
306 0 1 2.7E-03 0 0
CUI: C4551915
Disease: Gait Disturbance, CTCAE
Gait Disturbance, CTCAE
299 0 1 2.7E-03 0 0
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
294 0 1 2.7E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
291 0 1 2.8E-03 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot
285 0 1 2.8E-03 0 0
CUI: C1865014
Disease: Long philtrum
Long philtrum
282 0 1 2.8E-03 0 0
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
272 0 1 2.9E-03 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
955 0 3 2.9E-03 0 0
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
610 0 2 2.9E-03 0 0