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: C1855648
Disease: KENNY-CAFFEY SYNDROME, TYPE 1
KENNY-CAFFEY SYNDROME, TYPE 1 		2 0 2 0.50 0 0
CUI: C4316787
Disease: Kenny-Caffey syndrome, type 2
Kenny-Caffey syndrome, type 2 		2 0 2 0.50 0 0
CUI: C1855657
Disease: Calvarial osteosclerosis
Calvarial osteosclerosis 		3 0 2 0.40 0 0
CUI: C1859449
Disease: Thin long bone diaphyses
Thin long bone diaphyses 		3 0 2 0.40 0 0
CUI: C4022179
Disease: Stenosis of the medullary cavity of the long bones
Stenosis of the medullary cavity of the long bones 		3 0 2 0.40 0 0
CUI: C0151940
Disease: Hypocalcemic tetany
Hypocalcemic tetany 		4 0 2 0.33 0 0
CUI: C1455734
Disease: Congenital hypoparathyroidism
Congenital hypoparathyroidism 		5 0 2 0.29 0 0
CUI: C0015263
Disease: Bronchospasm, Exercise-Induced
Bronchospasm, Exercise-Induced 		1 0 1 0.25 0 0
CUI: C0037942
Disease: Spinal Osteophytosis
Spinal Osteophytosis 		1 0 1 0.25 0 0
CUI: C0156318
Disease: Fibrosclerosis of breast
Fibrosclerosis of breast 		1 0 1 0.25 0 0
CUI: C0221745
Disease: Depression suicidal
Depression suicidal 		1 0 1 0.25 0 0
CUI: C0265291
Disease: Kenny-Caffey syndrome
Kenny-Caffey syndrome 		6 0 2 0.25 0 0
CUI: C0585473
Disease: Chondromyxoid fibroma of bone
Chondromyxoid fibroma of bone 		1 0 1 0.25 0 0
CUI: C0878576
Disease: Posterior Leukoencephalopathy Syndrome
Posterior Leukoencephalopathy Syndrome 		1 0 1 0.25 0 0
CUI: C1275239
Disease: Dermatomyofibroma
Dermatomyofibroma 		1 0 1 0.25 0 0
CUI: C1290073
Disease: Acute mucositis
Acute mucositis 		1 0 1 0.25 0 0
CUI: C1335169
Disease: Ovarian Adenosarcoma
Ovarian Adenosarcoma 		1 0 1 0.25 0 0
CUI: C1394142
Disease: Cortical hyperostosis
Cortical hyperostosis 		1 0 1 0.25 0 0
CUI: C1832273
Disease: Ribbing disease
Ribbing disease 		1 0 1 0.25 0 0
CUI: C1834345
Disease: Periosteal thickening of long tubular bones
Periosteal thickening of long tubular bones 		1 0 1 0.25 0 0
CUI: C1851612
Disease: Narrowing of medullary canal
Narrowing of medullary canal 		1 0 1 0.25 0 0
CUI: C1852924
Disease: OI-EDS Combined Syndrome
OI-EDS Combined Syndrome 		1 0 1 0.25 0 0
CUI: C1855840
Disease: HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME
HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME 		1 0 1 0.25 0 0
CUI: C1859069
Disease: Brittle Bone Disorder
Brittle Bone Disorder 		1 0 1 0.25 0 0
CUI: C1865639
Disease: Gracile bone dysplasia
Gracile bone dysplasia 		1 0 1 0.25 0 0