ORPHA:2641
OBSOLETE: Micromelic dwarfism, Fryns type
inactive · referred to ORPHA:254Spondylometaphyseal dysplasia
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Spondylometaphyseal dysplasia
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Micromelic dwarfism, Fryns type | |
| fr | OBSOLETE : Nanisme micromélique type Fryns | |
| de | OBSOLET: Kleinwuchs, mikromeler, Typ Fryns | |
| es | OBSOLETO: Talla baja significativa micromélica tipo Fryns | OBSOLETO: Enanismo micromélico tipo Fryns |
| it | OBSOLETO: Nanismo micromelico, tipo Fryns | |
| nl | OBSOLEET: Micromelische dwerggroei, Fryns-type | |
| pt | OBSOLETO: Nanismo micromélico, tipo Fryns | |
| pl | NIEAKTUALNE: Niskoroslosc mikromeliczna typu Frynsa | |
| cs | NEAKTUÁLNÍ: Mikromelické trpaslictví, Frynsův typ | |
| uk | ЗАСТАРІЛО: Мікромелічна карликовість, тип Фрінса | |
| zh | 弃用：细肢性侏儒症，Fryns型 | |
| tr | Eski adı: Mikromelik cücelik, Fryns tipi |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2641
- This record as JSON: /data/d/2641.json