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: C1849265
Disease: Overgrowth
Overgrowth 		103 0 8 6.6E-02 0 0
CUI: C0271708
Disease: Fasting Hypoglycemia
Fasting Hypoglycemia 		39 0 4 6.5E-02 0 0
CUI: C1836674
Disease: Short distal phalanx of the 5th finger
Short distal phalanx of the 5th finger 		6 0 2 6.5E-02 0 0
CUI: C1839271
Disease: Birth length greater than 97th percentile
Birth length greater than 97th percentile 		6 0 2 6.5E-02 0 0
CUI: C0009677
Disease: Congenital macroglossia
Congenital macroglossia 		7 0 2 6.2E-02 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 4 6.2E-02 0 0
CUI: C0796113
Disease: Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor 		7 0 2 6.2E-02 0 0
CUI: C1850087
Disease: Narrow sacroiliac notch
Narrow sacroiliac notch 		7 0 2 6.2E-02 0 0
CUI: C1862142
Disease: Short 2nd finger
Short 2nd finger 		7 0 2 6.2E-02 0 0
CUI: C1854928
Disease: Protuberant abdomen
Protuberant abdomen 		25 0 3 6.1E-02 0 0
CUI: C0162510
Disease: Caroli Disease
Caroli Disease 		8 0 2 6.1E-02 0 0
CUI: C0238577
Disease: Abdominal wall defect
Abdominal wall defect 		8 0 2 6.1E-02 0 0
CUI: C0267834
Disease: Liver cyst
Liver cyst 		26 0 3 6.0E-02 0 0
CUI: C0020258
Disease: Hydrocephalus, Normal Pressure
Hydrocephalus, Normal Pressure 		44 0 4 6.0E-02 0 0
CUI: C0796154
Disease: SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1 		44 0 4 6.0E-02 0 0
CUI: C0266619
Disease: Potter's facies
Potter's facies 		9 0 2 5.9E-02 0 0
CUI: C0268146
Disease: Glucose-6-phosphate transport defect
Glucose-6-phosphate transport defect 		9 0 2 5.9E-02 0 0
CUI: C0432055
Disease: Simple syndactyly of fingers - first web
Simple syndactyly of fingers - first web 		9 0 2 5.9E-02 0 0
CUI: C0677608
Disease: Chorioangioma
Chorioangioma 		9 0 2 5.9E-02 0 0
CUI: C1832983
Disease: Absent or minimally ossified vertebral bodies
Absent or minimally ossified vertebral bodies 		9 0 2 5.9E-02 0 0
CUI: C1867114
Disease: Craniofacial disproportion
Craniofacial disproportion 		9 0 2 5.9E-02 0 0
CUI: C2939174
Disease: Medullary cystic disease
Medullary cystic disease 		9 0 2 5.9E-02 0 0
CUI: C4317043
Disease: Simpson-Golabi-Behmel syndrome
Simpson-Golabi-Behmel syndrome 		9 0 2 5.9E-02 0 0
CUI: C4554010
Disease: Isomerism (body)
Isomerism (body) 		9 0 2 5.9E-02 0 0
CUI: C0431718
Disease: Multiple renal cysts
Multiple renal cysts 		46 0 4 5.8E-02 0 0