ORPHA:1894
Ectrodactyly-spina bifida-cardiopathy syndrome
inactive · moved to ORPHA:2008Acrocardiofacial syndrome
Synonyms: Kasznica-Carlson-Coppedge syndrome
- 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 Acrocardiofacial syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Ectrodactyly-spina bifida-cardiopathy syndrome | Kasznica-Carlson-Coppedge syndrome |
| fr | Syndrome d'ectrodactylie-spina bifida-cardiopathie | Syndrome de Kasznica-Carlson-Coppedge |
| de | Ektrodaktylie-Spina bifida-Kardiopathie-Syndrom | Kasznica-Carlson-Coppedge-Syndrom |
| es | Síndrome de ectrodactilia-espina bífida-cardiopatía | Síndrome de Kasznica-Carlson-Coppedge |
| it | Ectrodattilia - spina bifida - cardiopatia | Sindrome di Kasznica-Carlson-Coppedge |
| nl | Ectrodactylie - spina bifida - cardiopathie-syndroom | Syndroom van Kasznica-Carlson-Coppedge |
| pt | Síndrome de ectrodactilia-espinha bífida-cardiopatia | Síndrome Kasznica-Carlson-Coppedge |
| pl | Ektrodaktylia - rozszczep kręgosłupa - kardiopatia | Zespół Kasznica, Carlsona i Coppedge'a |
| cs | Syndrom zahrnující ektrodaktylii, spina bifida a kardiomyopatii | Kasznicaův-Carlsonův-Coppedgeův syndrom · Kasznica-Carlson-Coppedgeův syndrom |
| uk | Синдром ектродактилії-spina bifida-кардіопатії | Синдром Кашніца-Карлсона-Коппеджа |
| zh | 缺指畸形-脊柱裂-心脏病综合征 | Kasznica-Carlson-Coppedge 综合征 |
| tr | Ektrodaktili-spina bifida-kardiyopati sendromu | Kasznica-Carlson-Coppedge sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C2931393 | 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/1894
- This record as JSON: /data/d/1894.json