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: C0040261
Disease: Onychomycosis
Onychomycosis 		27 0 8 9.3E-02 0 0
CUI: C1535950
Disease: Gastrointestinal inflammation
Gastrointestinal inflammation 		39 0 9 9.3E-02 0 0
CUI: C0342751
Disease: Generalized glycogen storage disease of infants
Generalized glycogen storage disease of infants 		51 0 10 9.3E-02 0 0
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 0 9 9.2E-02 0 0
CUI: C0022346
Disease: Icterus
Icterus 		241 0 25 8.8E-02 0 0
CUI: C0033774
Disease: Pruritus
Pruritus 		107 0 14 8.7E-02 0 0
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice 		59 14 10 8.6E-02 1 5.3E-02
CUI: C3805574
Disease: Increased fracture rate
Increased fracture rate 		123 0 15 8.6E-02 0 0
CUI: C3887650
Disease: Adult Rickets
Adult Rickets 		47 0 9 8.6E-02 0 0
CUI: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection 		9 0 6 8.6E-02 0 0
CUI: C1854111
Disease: Broad philtrum
Broad philtrum 		22 0 7 8.5E-02 0 0
CUI: C0151480
Disease: Anti-nuclear factor positive
Anti-nuclear factor positive 		35 0 8 8.5E-02 0 0
CUI: C1837732
Disease: Thickened helices
Thickened helices 		37 0 8 8.3E-02 0 0
CUI: C1859461
Disease: Femoral bowing
Femoral bowing 		38 13 8 8.2E-02 1 5.6E-02
CUI: C0694563
Disease: Excessive daytime somnolence
Excessive daytime somnolence 		39 0 8 8.2E-02 0 0
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia 		53 0 9 8.1E-02 0 0
CUI: C0860218
Disease: ABO incompatibility
ABO incompatibility 		14 0 6 8.0E-02 0 0
CUI: C1833325
Disease: Thin bony cortex
Thin bony cortex 		14 0 6 8.0E-02 0 0
CUI: C1384670
Disease: Single umbilical artery
Single umbilical artery 		28 0 7 8.0E-02 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 9 7.9E-02 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 10 7.9E-02 0 0
CUI: C1704375
Disease: Hypophosphatemic Rickets
Hypophosphatemic Rickets 		29 0 7 7.9E-02 0 0
CUI: C2677328
Disease: Cerebral hypomyelination
Cerebral hypomyelination 		29 0 7 7.9E-02 0 0
CUI: C3536983
Disease: Familial Hypophosphatemic Rickets
Familial Hypophosphatemic Rickets 		43 15 8 7.8E-02 1 5.0E-02
CUI: C4021757
Disease: EEG with polyspike wave complexes
EEG with polyspike wave complexes 		30 0 7 7.8E-02 0 0