ORPHA:324999
JMP syndrome
inactive · moved to ORPHA:324977Proteasome-associated autoinflammatory syndrome
Synonyms: Joint contractures-muscular atrophy-microcytic anemia-panniculitis-associated lipodystrophy syndrome
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Proteasome-associated autoinflammatory syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | JMP syndrome | Joint contractures-muscular atrophy-microcytic anemia-panniculitis-associated lipodystrophy syndrome |
| fr | Syndrome JMP | Syndrome de contractures articulaires-atrophie musculaire-anémie microcytique-panniculite lipoatrophiante |
| de | JMP-Syndrom | Gelenkkontrakturen-Muskelatrophie-mikrozytische Anämie-Pannikulitis-assoziierte Lipodystrophie-Syndrom |
| es | Síndrome JMP | Síndrome contracturas articulares-atrofia muscular-anemia microcítica-lipodistrofia asociada a paniculitis |
| it | Sindrome JMP | Sindrome contratture articolari-atrofia muscolare-anemia microcitica-panniculite associata a lipodistrofia |
| nl | JMP-syndroom | Gewrichtscontracturen - musculaire atrofie - microcytaire anemie - panniculitis - geassocieerde lipodystrofie-syndroom |
| pt | Síndrome JMP | |
| pl | Zespół JMP | Zespół przykurcze stawów-atrofia mięśni-niedokrwistość mikrocytarna-zapalenie tkanki tłuszczowej-lipodystrofia towarzysząca |
| cs | JMP syndrom | Syndrom zahrnující kloubní kontraktury, svalovou atrofii, mikrocytární anémii a lipodystrofii indukovanou panikulitidou |
| uk | Синдром JMP | Синдром контрактур суглобів - мязової атрофії - мікроцитарної анемії - паннікуліту - асоційованої ліподистрофії |
| zh | 自身炎症,脂肪营养不良和皮肤病综合征 | 关节挛缩-肌肉萎缩-小细胞性贫血-脂膜炎相关脂质营养不良综合征 |
| tr | JMP sendromu | Eklem kontraktürleri-müsküler atrofi-mikrositik anemi-pannikülit ile ilişkili lipodistrofi sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| GARD | 10988 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/324999
- This record as JSON: /data/d/324999.json