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: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 3.8E-03 0 0
CUI: C0042798
Disease: Low Vision
Low Vision 		157 0 1 3.8E-03 0 0
CUI: C3468561
Disease: familial atrial fibrillation
familial atrial fibrillation 		157 0 1 3.8E-03 0 0
CUI: C2585653
Disease: Persistent atrial fibrillation
Persistent atrial fibrillation 		156 0 1 3.8E-03 0 0
CUI: C0240063
Disease: Coloboma of iris
Coloboma of iris 		153 0 1 3.8E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 1 3.8E-03 0 0
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		149 0 1 3.9E-03 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris 		148 0 1 3.9E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency 		148 0 1 3.9E-03 0 0
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		147 0 1 3.9E-03 0 0
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		147 0 1 3.9E-03 0 0
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		147 0 1 3.9E-03 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy 		146 0 1 3.9E-03 0 0
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		401 0 2 3.9E-03 0 0
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		145 0 1 4.0E-03 0 0
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		653 0 3 4.0E-03 0 0
CUI: C0424678
Disease: Lean body mass
Lean body mass 		144 0 1 4.0E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial 		142 0 1 4.0E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		385 0 2 4.1E-03 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		137 0 1 4.1E-03 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		137 0 1 4.1E-03 0 0
CUI: C0266589
Disease: Congenital ear anomaly NOS (disorder)
Congenital ear anomaly NOS (disorder) 		137 0 1 4.1E-03 0 0
CUI: C1963094
Disease: Dry Skin, CTCAE
Dry Skin, CTCAE 		137 0 1 4.1E-03 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 1 4.1E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 0 1 4.1E-03 0 0