ORPHA:93686
OBSOLETE: Multicentric Castleman disease
inactive · referred to ORPHA:160Castleman disease
Synonyms: OBSOLETE: MCD · OBSOLETE: Multicentric giant lymph node hyperplasia
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Castleman disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Multicentric Castleman disease | OBSOLETE: MCD · OBSOLETE: Multicentric giant lymph node hyperplasia |
| fr | OBSOLETE : Maladie de Castleman multicentrique | OBSOLETE : Hyperplasie ganglionnaire géante multicentrique · OBSOLETE : MCM |
| de | OBSOLET: Multizentrische Castleman-Krankheit | OBSOLET: MCD · OBSOLET: Multizentrische Riesenganglien-Hyperplasie |
| es | OBSOLETO: Enfermedad de Castleman multicéntrica | OBSOLETO: ECM · OBSOLETO: Hiperplasia de ganglio linfático gigante multicéntrica |
| it | OBSOLETO: Malattia multicentrica di Castleman | OBSOLETE: MCD · OBSOLETO: Iperplasia multicentrica gigante dei linfonodi |
| nl | OBSOLEET: Multicentrische ziekte van Castleman | OBSOLEET: MCD · OBSOLEET: Multicentrische reuzenlymfeklierhyperplasie |
| pt | OBSOLETO: Doença de Castleman multicêntrica (MCD) | |
| pl | NIEAKTUALNE: Wielocentryczna choroba Castelmana | NIEAKTUALNE: MCD · NIEAKTUALNE: Wielocentryczny olbrzymi przerost węzłów chłonnych |
| cs | NEAKTUÁLNÍ: Multicentrická Castlemanova choroba | NEAKTUÁLNÍ: MCD · NEAKTUÁLNÍ: Multicentrická hyperplázie mízních uzlin |
| uk | ЗАСТАРІЛО: Мультицентрична хвороба Кастлмана | ЗАСТАРІЛО: MCD · ЗАСТАРІЛО: Мультицентрична гігантська гіперплазія лімфатичних вузлів |
| zh | 弃用:多中心型Castleman病 | 多中心巨淋巴结增生症 |
| tr | Eski adı: Çoklu Castleman hastalığı | MCD · Çok merkezli dev lenf düğümü hiperplazisi |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/93686
- This record as JSON: /data/d/93686.json