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: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly
1 0 1 1.8E-03 0 0
CUI: C0158651
Disease: Cleft lip, unilateral, complete
Cleft lip, unilateral, complete
1 0 1 1.8E-03 0 0
CUI: C0158983
Disease: Neonatal thyrotoxicosis
Neonatal thyrotoxicosis
1 0 1 1.8E-03 0 0
CUI: C0159104
Disease: Electrooculogram abnormal
Electrooculogram abnormal
1 0 1 1.8E-03 0 0
CUI: C0206619
Disease: Lymphatic Vessel Tumors
Lymphatic Vessel Tumors
1 0 1 1.8E-03 0 0
CUI: C0206649
Disease: Neoplasms, Fibroepithelial
Neoplasms, Fibroepithelial
1 0 1 1.8E-03 0 0
CUI: C0221151
Disease: Projectile vomiting
Projectile vomiting
1 0 1 1.8E-03 0 0
CUI: C0232567
Disease: Hypergastrinemia
Hypergastrinemia
1 0 1 1.8E-03 0 0
CUI: C0233283
Disease: Complete breech presentation
Complete breech presentation
1 0 1 1.8E-03 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation
1 0 1 1.8E-03 0 0
CUI: C0233623
Disease: Onychotillomania
Onychotillomania
1 0 1 1.8E-03 0 0
CUI: C0234505
Disease: Tactile Agnosia
Tactile Agnosia
1 0 1 1.8E-03 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction
1 0 1 1.8E-03 0 0
CUI: C0238185
Disease: Juvenile myxedema
Juvenile myxedema
1 0 1 1.8E-03 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing
1 0 1 1.8E-03 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff
1 0 1 1.8E-03 0 0
CUI: C0241633
Disease: Vaginal dryness
Vaginal dryness
1 0 1 1.8E-03 0 0
CUI: C0265113
Disease: Progressing stroke
Progressing stroke
1 0 1 1.8E-03 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome
1 0 1 1.8E-03 0 0
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A
1 0 1 1.8E-03 0 0
Knuckle pads, leuconychia and sensorineural deafness
1 21 1 1.8E-03 1 4.7E-03
CUI: C0266357
Disease: Persistent umbilical sinus
Persistent umbilical sinus
1 0 1 1.8E-03 0 0
CUI: C0267430
Disease: Noninfectious colitis
Noninfectious colitis
1 0 1 1.8E-03 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome
1 0 1 1.8E-03 0 0
Inherited disorder of bilirubin metabolism
1 0 1 1.8E-03 0 0