ORPHA:2725
Eye defects-arachnodactyly-cardiopathy syndrome
inactive · moved to ORPHA:642099Spondyloepimetaphyseal dysplasia with joint laxity, Beighton type
Synonyms: Al Gazali-Al Talabani syndrome · Al Gazali-Lytle 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 Spondyloepimetaphyseal dysplasia with joint laxity, Beighton type
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Eye defects-arachnodactyly-cardiopathy syndrome | Al Gazali-Al Talabani syndrome · Al Gazali-Lytle syndrome |
| fr | Syndrome d'anomalie de l'oeil-arachnodactylie-cardiopathie | Syndrome d'Al Gazali-Al Talabani · Syndrome d'Al Gazali-Lytle |
| de | Augendefekte-Arachnodaktylie-Kardiopathie-Syndrom | Al-Gazali-al-Talabani-Syndrom |
| es | Síndrome de anomalía ocular-aracnodactilia-cardiopatía | Síndrome de Al Gazali-Al Talabani · Síndrome de Al Gazali-Lytle |
| it | Sindrome anomalie oculari-aracnodattilia-cardiopatia | Sindrome di Al Gazali-Al Talabani · Sindrome di Al Gazali-Lytle |
| nl | Oogdefecten - arachnodactylie - cardiopathie-syndroom | Syndroom van Al Gazali-Al Talabani · Syndroom van Al Gazali-Lytle |
| pt | Síndrome de anomalias oculares-aracnodactilia-cardiopatia | Síndrome Al Gazali-Al Talabani |
| pl | Wady oka - arachnodaktylia - kardiopatia | Zespół Al Gazali i Al Talabani · Zespół Al Gazali i Lytle |
| cs | Syndrom zahrnující defekty očí, arachnodaktylii a kardiopatii | Al Gazaliové-Al Talabaniové syndrom · Al Gazaliové-Lytleův syndrom · Al Gazali-Al Talabaniové syndrom · Al Gazali-Lytleův syndrom |
| uk | Синдром дефекту очей-арахнодактилії-кардіопатії | Синдром Аль Газалі Аль Талабані · Синдром Аль-Газалі-Лайта |
| zh | 眼部缺陷-蜘蛛样指-心脏病综合征 | Al Gazali-Al Talabani综合征 |
| tr | Göz defektleri-araknodaktili-kardiyopati sendromu | Al Gazali-Lytle sendromu · Al Gazali-Al Talabani sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 609465 | E | validated | |
| GARD | 10054 | 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/2725
- This record as JSON: /data/d/2725.json