ORPHA:2646
Parastremmatic dysplasia
inactive · moved to ORPHA:263482Spondyloepimetaphyseal dysplasia, Maroteaux type
Synonyms: Parastremmatic dwarfism
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Spondyloepimetaphyseal dysplasia, Maroteaux type
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Parastremmatic dysplasia | Parastremmatic dwarfism |
| fr | Dysplasie parastremmatique | Nanisme parastremmatique |
| de | Kleinwuchs, parastrematischer | Dysplasie, parastrematische |
| es | Displasia parastremática | Enanismo parastremático |
| it | Displasia parastremmatica | Nanismo parastremmatico |
| nl | Parastremmatische dysplasie | Parastremmatische dwerggroei |
| pt | Displasia parastremática | Nanismo parastremático |
| pl | Dysplazja parastrematyczna | = en |
| cs | Parastrematické trpaslictví | = en |
| uk | Парастрематична дисплазія | Парастрематична карликовість |
| zh | 类扭伤性侏儒症 | |
| tr | Parastremmatik cücelik |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 168400 | E | validated | |
| MONDO | 0008196 | E | validated | |
| MeSH | C537172 | E | validated | |
| UMLS | C1868616 | E | validated | |
| GARD | 4222 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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/2646
- This record as JSON: /data/d/2646.json