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: C0000729
Disease: Abdominal Cramps
Abdominal Cramps 		1 0 1 9.6E-03 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 9.6E-03 0 0
CUI: C0004048
Disease: Inspiration function
Inspiration function 		1 0 1 9.6E-03 0 0
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 9.6E-03 0 0
CUI: C0031925
Disease: Pilonidal Cyst
Pilonidal Cyst 		1 0 1 9.6E-03 0 0
CUI: C0034882
Disease: Rectal Diseases
Rectal Diseases 		1 0 1 9.6E-03 0 0
CUI: C0036413
Disease: Scleredema Adultorum
Scleredema Adultorum 		1 0 1 9.6E-03 0 0
CUI: C0038557
Disease: Submandibular Gland Diseases
Submandibular Gland Diseases 		1 0 1 9.6E-03 0 0
CUI: C0040422
Disease: Tonsillar Neoplasms
Tonsillar Neoplasms 		1 0 1 9.6E-03 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 9.6E-03 0 0
CUI: C0153614
Disease: Malignant neoplasm of ureteric orifice
Malignant neoplasm of ureteric orifice 		1 0 1 9.6E-03 0 0
CUI: C0153618
Disease: Malignant tumor of renal pelvis
Malignant tumor of renal pelvis 		1 0 1 9.6E-03 0 0
CUI: C0155930
Disease: Tooth Ankylosis
Tooth Ankylosis 		1 0 1 9.6E-03 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 9.6E-03 0 0
CUI: C0220743
Disease: Childhood hypophosphatasia (disorder)
Childhood hypophosphatasia (disorder) 		1 0 1 9.6E-03 0 0
CUI: C0221360
Disease: Congenital absence of diaphragm
Congenital absence of diaphragm 		1 0 1 9.6E-03 0 0
CUI: C0231450
Disease: Abnormal extension
Abnormal extension 		1 0 1 9.6E-03 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 9.6E-03 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain 		1 0 1 9.6E-03 0 0
CUI: C0241060
Disease: Cyst of skin
Cyst of skin 		1 0 1 9.6E-03 0 0
CUI: C0241136
Disease: Pain of skin
Pain of skin 		1 0 1 9.6E-03 0 0
CUI: C0259782
Disease: Telangiectatic osteosarcoma
Telangiectatic osteosarcoma 		1 0 1 9.6E-03 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 9.6E-03 0 0
CUI: C0264081
Disease: Osteoarthropathy of fingers familial
Osteoarthropathy of fingers familial 		1 0 1 9.6E-03 0 0
CUI: C0265263
Disease: Femoral hypoplasia - unusual facies syndrome
Femoral hypoplasia - unusual facies syndrome 		1 0 1 9.6E-03 0 0