Ollier disease
Sign in to saveAlso known as DYSCHONDROPLASIA, ENCHONDROMATOSIS, MULTIPLE, Enchondromatosis with haemangiomata, Kast's syndrome, OSTEOCHONDROMATOSIS
rare nonhereditary sporadic disorder
In the Vinony graph
Within Vinony's link graph, Ollier disease is referenced by 62 other articles, and connects out to International Standard Book Number, digital object identifier and International Standard Serial Number.
It is catalogued under topics including Genetic disorders with OMIM but no gene, Rare diseases and Skeletal disorders.
Its subject is documented across 9 Wikipedia language editions.
Wikidata facts
- Subclass of
- disease
Show 6 more facts
- Commons category
- Ollier disease
- health specialty
- medical genetics
- symptoms and signs
- enchondromatosis
- NCI Thesaurus ID
- C3213
- exact match
- www.orpha.net/ORDO/Orphanet_296
- on focus list of Wikimedia project
- WikiProject Medicine
Sources (2)
via Wikidata · CC0
Connections
International Standard Book Number
Entity
digital object identifier
Entity
International Standard Serial Number
Entity
central nervous system
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magnetic resonance imaging
Entity
bone fracture
Disease
surgeon
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PubMed
Entity
International Statistical Classification of Diseases and Related Health Problems
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dwarfism
Disease
radius
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PubMed Central
Entity
Medical Subject Headings
Entity
achondroplasia
Entity
medical specialty
Entity
sarcoma
Entity
Online Mendelian Inheritance in Man
Entity
Diseases Database
Entity
eMedicine
Entity
ICD-10
Entity