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 2.0E-02 0 0
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 2.0E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 2.0E-02 0 0
CUI: C0155930
Disease: Tooth Ankylosis
Tooth Ankylosis 		1 0 1 2.0E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 2.0E-02 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 2.0E-02 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain 		1 0 1 2.0E-02 0 0
CUI: C0264081
Disease: Osteoarthropathy of fingers familial
Osteoarthropathy of fingers familial 		1 0 1 2.0E-02 0 0
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A 		1 0 1 2.0E-02 0 0
CUI: C0265280
Disease: Spondylometaphyseal dysplasia, Kozlowski type
Spondylometaphyseal dysplasia, Kozlowski type 		1 0 1 2.0E-02 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism 		1 0 1 2.0E-02 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 2.0E-02 0 0
CUI: C0271869
Disease: Pseudohypoparathyroidism type I B
Pseudohypoparathyroidism type I B 		1 0 1 2.0E-02 0 0
CUI: C0332885
Disease: Congenital stenosis
Congenital stenosis 		1 0 1 2.0E-02 0 0
CUI: C0340031
Disease: Mucociliary clearance defect
Mucociliary clearance defect 		1 0 1 2.0E-02 0 0
CUI: C0345286
Disease: Abnormal liver lobulation
Abnormal liver lobulation 		1 0 1 2.0E-02 0 0
CUI: C0392176
Disease: Gastric irritation
Gastric irritation 		1 0 1 2.0E-02 0 0
CUI: C0392445
Disease: Necrobiosis Lipoidica Diabeticorum
Necrobiosis Lipoidica Diabeticorum 		1 0 1 2.0E-02 0 0
CUI: C0431691
Disease: Unilateral Renal Hypoplasia
Unilateral Renal Hypoplasia 		1 0 1 2.0E-02 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 2.0E-02 0 0
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3 		1 0 1 2.0E-02 0 0
CUI: C0478093
Disease: Other congenital malformation syndromes with other skeletal changes
Other congenital malformation syndromes with other skeletal changes 		1 0 1 2.0E-02 0 0
CUI: C0562557
Disease: Sexually disinhibited behavior
Sexually disinhibited behavior 		1 0 1 2.0E-02 0 0
CUI: C0575827
Disease: Small finger
Small finger 		1 0 1 2.0E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 2.0E-02 0 0