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: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0 152 0 0 1 6.3E-03
CUI: C0038379
Disease: Strabismus
Strabismus
716 0 1 1.3E-03 0 0
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
620 0 1 1.5E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
580 0 1 1.6E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
568 0 1 1.6E-03 0 0
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders
560 0 1 1.6E-03 0 0
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
546 0 1 1.7E-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 1.9E-03 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
955 0 2 2.0E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
433 0 1 2.1E-03 0 0
CUI: C1836542
Disease: Depressed nasal bridge
Depressed nasal bridge
426 0 1 2.1E-03 0 0
CUI: C3665347
Disease: Visual Impairment
Visual Impairment
422 0 1 2.1E-03 0 0
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus
417 0 1 2.1E-03 0 0
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril
407 0 1 2.2E-03 0 0
Corpuscular Hemoglobin Concentration Mean
401 0 1 2.2E-03 0 0
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure
391 0 1 2.3E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 0 2 2.3E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum
385 0 1 2.3E-03 0 0
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis
376 0 1 2.3E-03 0 0
CUI: C0221355
Disease: Macrocephaly
Macrocephaly
367 0 1 2.4E-03 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0
779 0 2 2.4E-03 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0
779 0 2 2.4E-03 0 0
CUI: C1384666
Disease: hearing impairment
hearing impairment
740 0 2 2.5E-03 0 0
CUI: C0221357
Disease: Brachydactyly
Brachydactyly
325 0 1 2.7E-03 0 0