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: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 5.7E-03 0 0
CUI: C0003467
Disease: Anxiety
Anxiety 		1048 0 1 9.5E-04 0 0
CUI: C0004134
Disease: Ataxia
Ataxia 		868 0 1 1.2E-03 0 0
CUI: C0009421
Disease: Comatose
Comatose 		78 0 1 1.3E-02 0 0
CUI: C0009676
Disease: Confusion
Confusion 		75 0 1 1.3E-02 0 0
CUI: C0011206
Disease: Delirium
Delirium 		110 0 1 9.1E-03 0 0
CUI: C0011991
Disease: Diarrhea
Diarrhea 		632 0 1 1.6E-03 0 0
CUI: C0013144
Disease: Drowsiness
Drowsiness 		31 0 1 3.2E-02 0 0
CUI: C0013528
Disease: Echolalia
Echolalia 		39 0 1 2.6E-02 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		842 0 1 1.2E-03 0 0
CUI: C0015672
Disease: Fatigue
Fatigue 		760 0 1 1.3E-03 0 0
CUI: C0018681
Disease: Headache
Headache 		338 0 1 3.0E-03 0 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		523 0 1 1.9E-03 0 0
CUI: C0021290
Disease: Neonatal disorder
Neonatal disorder 		15 0 1 6.7E-02 0 0
CUI: C0023380
Disease: Lethargy
Lethargy 		160 0 1 6.3E-03 0 0
CUI: C0025521
Disease: Inborn Errors of Metabolism
Inborn Errors of Metabolism 		119 0 1 8.4E-03 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly 		1064 0 1 9.4E-04 0 0
CUI: C0026985
Disease: Myelodysplasia
Myelodysplasia 		181 0 1 5.5E-03 0 0
CUI: C0027497
Disease: Nausea
Nausea 		161 0 1 6.2E-03 0 0
CUI: C0030486
Disease: Paraplegia
Paraplegia 		59 0 1 1.7E-02 0 0
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias 		83 0 1 1.2E-02 0 0
CUI: C0036572
Disease: Seizures
Seizures 		2152 0 1 4.6E-04 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		135 0 1 7.4E-03 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		192 0 1 5.2E-03 0 0
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		1658 0 1 6.0E-04 0 0