ORPHA:370019
Spondylometaphyseal dysplasia, Czarny-Ratajczak type
inactive · moved to ORPHA:168555Spondylometaphyseal dysplasia, A4 type
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Spondylometaphyseal dysplasia, A4 type
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Spondylometaphyseal dysplasia, Czarny-Ratajczak type | |
| fr | Dysplasie spondylo-métaphysaire type Czarny-Ratajczak | |
| de | Dysplasie, spondyloepimetaphysäre, Typ Czarny-Ratajczak | |
| es | Displasia espondilometafisaria tipo Czarny-Ratajczak | |
| it | Displasia spondilometafisaria tipo Czarny-Ratajczak | |
| nl | Spondylometafysaire dysplasie, Czarny-Ratajczak-type | |
| pt | Displasia espondilometafisária, tipo Czarny-Ratajczak | |
| pl | Dysplazja kręgowo-nasadowa typu Czarny-Ratajczak | |
| cs | Spondyloepimetafyzární dysplázie, typ Czarny-Ratajczak | |
| uk | Спондилометафізарна дисплазія, тип Чарні-Ратайчака | |
| zh | Czarny-Ratajczak型脊柱-上肢-干骺端发育不良 | |
| tr | Spondilometafizyal displazi, Czarny-Ratajczak tipi |
Definition in:
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/370019
- This record as JSON: /data/d/370019.json