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: C4024188
Disease: Curved distal phalanges of the hand
Curved distal phalanges of the hand
2 0 2 0.33 0 0
CUI: C0020496
Disease: Hyperostosis of skull
Hyperostosis of skull
4 0 2 0.25 0 0
CUI: C0265301
Disease: Sclerosteosis
Sclerosteosis
7 0 2 0.18 0 0
CUI: C0021355
Disease: Infective otitis externa
Infective otitis externa
1 0 1 0.17 0 0
CUI: C0152008
Disease: Vulvovaginal disease
Vulvovaginal disease
1 0 1 0.17 0 0
CUI: C0157680
Disease: Carbuncle/furuncle
Carbuncle/furuncle
1 0 1 0.17 0 0
CUI: C0232495
Disease: Lower abdominal pain
Lower abdominal pain
1 0 1 0.17 0 0
CUI: C0238454
Disease: Cavernous Sinus Thrombosis
Cavernous Sinus Thrombosis
1 0 1 0.17 0 0
CUI: C0259860
Disease: psychiatric emergencies
psychiatric emergencies
1 0 1 0.17 0 0
CUI: C0268493
Disease: Ochronotic arthritis
Ochronotic arthritis
1 0 1 0.17 0 0
CUI: C0332778
Disease: Diastasis, Bone
Diastasis, Bone
1 0 1 0.17 0 0
CUI: C0409224
Disease: Ochronotic arthropathy
Ochronotic arthropathy
1 0 1 0.17 0 0
CUI: C0409579
Disease: Rheumatic joint disease
Rheumatic joint disease
1 0 1 0.17 0 0
CUI: C0578437
Disease: Ischemic foot
Ischemic foot
1 0 1 0.17 0 0
CUI: C0854328
Disease: Infection due to anaerobic bacteria
Infection due to anaerobic bacteria
1 0 1 0.17 0 0
CUI: C0864813
Disease: Sporothrix schenckii Infection
Sporothrix schenckii Infection
1 0 1 0.17 0 0
Chronic lymphocytic leukaemia transformation
1 0 1 0.17 0 0
CUI: C1835697
Disease: Keratitis Fugax Hereditaria
Keratitis Fugax Hereditaria
1 0 1 0.17 0 0
Mental retardation X-linked, South African type
1 0 1 0.17 0 0
Facial palsy secondary to cranial hyperostosis
1 0 1 0.17 0 0
CUI: C1849263
Disease: Sclerotic scapulae
Sclerotic scapulae
1 0 1 0.17 0 0
CUI: C1849276
Disease: Cortically dense long tubular bones
Cortically dense long tubular bones
1 0 1 0.17 0 0
Pneumonia due to methicillin susceptible Staphylococcus aureus
1 0 1 0.17 0 0
CUI: C2931645
Disease: Ochronosis, hereditary
Ochronosis, hereditary
1 0 1 0.17 0 0
CUI: C3280402
Disease: SCLEROSTEOSIS 2
SCLEROSTEOSIS 2
1 0 1 0.17 0 0