Source: ALL
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: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 3.3E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 2.8E-02
CUI: C0333873
Disease: Squamous intraepithelial lesion
Squamous intraepithelial lesion 		0 8 0 0 1 2.7E-02
CUI: C0751007
Disease: Intracranial Atherosclerosis
Intracranial Atherosclerosis 		0 2 0 0 1 3.2E-02
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 3.2E-02
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder 		0 2 0 0 2 6.7E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		1156 0 1 8.1E-04 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		568 0 1 1.6E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		433 0 1 2.0E-03 0 0
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		401 0 1 2.1E-03 0 0
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		399 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: C0221355
Disease: Macrocephaly
Macrocephaly 		367 0 1 2.3E-03 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression 		333 0 1 2.4E-03 0 0
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency 		315 0 1 2.6E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 1 2.7E-03 0 0
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		653 0 2 2.7E-03 0 0
CUI: C1865014
Disease: Long philtrum
Long philtrum 		282 0 1 2.8E-03 0 0
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis 		281 0 1 2.8E-03 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		272 0 1 2.9E-03 0 0
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies 		271 0 1 2.9E-03 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		955 0 3 2.9E-03 0 0
CUI: C1854114
Disease: Short nose
Short nose 		265 0 1 2.9E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 3.1E-03 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		251 0 1 3.1E-03 0 0