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 5.4E-03 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type
1 0 1 5.4E-03 0 0
Childhood hypophosphatasia (disorder)
1 0 1 5.4E-03 0 0
CUI: C0221385
Disease: Syphilitic gumma
Syphilitic gumma
1 0 1 5.4E-03 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur
1 0 1 5.4E-03 0 0
CUI: C0232495
Disease: Lower abdominal pain
Lower abdominal pain
1 0 1 5.4E-03 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation
1 0 1 5.4E-03 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain
1 0 1 5.4E-03 0 0
CUI: C0235146
Disease: Euphoric mood
Euphoric mood
1 0 1 5.4E-03 0 0
Renal Pelvis Squamous Cell Carcinoma
1 0 1 5.4E-03 0 0
CUI: C0238479
Disease: Transient osteoporosis of hip
Transient osteoporosis of hip
1 0 1 5.4E-03 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria
1 0 1 5.4E-03 0 0
CUI: C0240583
Disease: Short upturned nose
Short upturned nose
1 0 1 5.4E-03 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities
1 0 1 5.4E-03 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus
1 0 1 5.4E-03 0 0
CUI: C0263925
Disease: Iliac crest spur
Iliac crest spur
1 0 1 5.4E-03 0 0
Osteoarthropathy of fingers familial
1 0 1 5.4E-03 0 0
CUI: C0264402
Disease: Gas bubble disease
Gas bubble disease
1 0 1 5.4E-03 0 0
CUI: C0265241
Disease: Franceschetti-Klein syndrome
Franceschetti-Klein syndrome
1 0 1 5.4E-03 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome
1 0 1 5.4E-03 0 0
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A
1 0 1 5.4E-03 0 0
Spondylometaphyseal dysplasia, Kozlowski type
1 11 1 5.4E-03 10 0.15
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism
1 19 1 5.4E-03 17 0.25
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome
1 0 1 5.4E-03 0 0
CUI: C0265512
Disease: Bone island
Bone island
1 0 1 5.4E-03 0 0