"Enchondromatosis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Benign growths of cartilage in the metaphyses of several bones.
| Descriptor ID |
D004687
|
| MeSH Number(s) |
C05.116.099.708.338
|
| Concept/Terms |
Enchondromatosis- Enchondromatosis
- Enchondromatoses
- Ollier's Disease
- Disease, Ollier's
- Olliers Disease
- Enchondrosis, Multiple
- Enchondroses, Multiple
- Multiple Enchondroses
- Multiple Enchondrosis
- Ollier Disease
- Disease, Ollier
- Enchondroma, Multiple
- Enchondromas, Multiple
- Multiple Enchondroma
- Multiple Enchondromas
- Enchondromatosis, Multiple
Maffucci Syndrome- Maffucci Syndrome
- Syndrome, Maffucci
- Enchondromatosis with Multiple Cavernous Hemangiomas
- Hemangiomatosis Chondrodystrophica
- Kast Syndrome
- Hemangiomata with Dyschondroplasia
- Chondrodysplasia with Hemangioma
- Chondroplasia Angiomatosis
- Dyschondroplasia and Cavernous Hemangioma
- Enchondromatosis with Hemangiomata
- Dyschondrodysplasia with Hemangiomas
- Multiple Angiomas and Endochondromas
|
Below are MeSH descriptors whose meaning is more general than "Enchondromatosis".
Below are MeSH descriptors whose meaning is more specific than "Enchondromatosis".
This graph shows the total number of publications written about "Enchondromatosis" by people in this website by year, and whether "Enchondromatosis" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 2 | 0 | 2 |
| 2011 | 1 | 1 | 2 |
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Below are the most recent publications written about "Enchondromatosis" by people in Profiles.
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Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2. Nat Genet. 2011 Nov 06; 43(12):1262-5.
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IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours. J Pathol. 2011 Jul; 224(3):334-43.
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Lack of HIF-2a in limb bud mesenchyme causes a modest and transient delay of endochondral bone development. Nat Med. 2011 Jan; 17(1):25-6; author reply 27-9.
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Multiple enchondromas associated with spindle-cell hemangioendotheliomas. An overlooked variant of Maffucci's syndrome. Am J Surg Pathol. 1995 Sep; 19(9):1029-38.
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Malignancy in Maffucci's syndrome. Dermatol Clin. 1995 Jan; 13(1):73-8.