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: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding) 		1 0 1 2.6E-03 0 0
CUI: C0221745
Disease: Depression suicidal
Depression suicidal 		1 0 1 2.6E-03 0 0
CUI: C0233283
Disease: Complete breech presentation
Complete breech presentation 		1 1 1 2.6E-03 1 2.0E-02
CUI: C0233623
Disease: Onychotillomania
Onychotillomania 		1 0 1 2.6E-03 0 0
CUI: C0234175
Disease: Palmar reflex
Palmar reflex 		1 0 1 2.6E-03 0 0
CUI: C0234435
Disease: Syncope, Tussive
Syncope, Tussive 		1 0 1 2.6E-03 0 0
CUI: C0234505
Disease: Tactile Agnosia
Tactile Agnosia 		1 0 1 2.6E-03 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction 		1 0 1 2.6E-03 0 0
CUI: C0235146
Disease: Euphoric mood
Euphoric mood 		1 0 1 2.6E-03 0 0
CUI: C0236688
Disease: Cocaine delirium
Cocaine delirium 		1 0 1 2.6E-03 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease 		1 0 1 2.6E-03 0 0
CUI: C0238525
Disease: Sarcoma of vulva
Sarcoma of vulva 		1 0 1 2.6E-03 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 2.6E-03 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 2.6E-03 0 0
CUI: C0262665
Disease: Abnormal vocal cord morphology
Abnormal vocal cord morphology 		1 2 1 2.6E-03 2 4.1E-02
CUI: C0263421
Disease: Acrodermatitis atrophicans chronica
Acrodermatitis atrophicans chronica 		1 0 1 2.6E-03 0 0
CUI: C0264558
Disease: Tension Pneumothorax
Tension Pneumothorax 		1 0 1 2.6E-03 0 0
CUI: C0265113
Disease: Progressing stroke
Progressing stroke 		1 0 1 2.6E-03 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 2.6E-03 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 2.6E-03 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus 		1 0 1 2.6E-03 0 0
CUI: C0266742
Disease: Asymmetrical conjoined twins
Asymmetrical conjoined twins 		1 0 1 2.6E-03 0 0
CUI: C0268262
Disease: Metachromatic Leukodystrophy due to Saposin B Deficiency
Metachromatic Leukodystrophy due to Saposin B Deficiency 		1 0 1 2.6E-03 0 0
CUI: C0268461
Disease: Disorder of phenylalanine metabolism
Disorder of phenylalanine metabolism 		1 0 1 2.6E-03 0 0
CUI: C0268603
Disease: Acetyl-CoA: carboxylase deficiency
Acetyl-CoA: carboxylase deficiency 		1 0 1 2.6E-03 0 0