ORPHA:1034
OBSOLETE: Amniotic bands
inactive · referred to ORPHA:498461Non-syndromic terminal transverse limb defect
Synonyms: OBSOLETE: ADAM syndrome · OBSOLETE: Amniotic deformity-adhesion-mutilation syndrome
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Non-syndromic terminal transverse limb defect
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Amniotic bands | OBSOLETE: ADAM syndrome · OBSOLETE: Amniotic deformity-adhesion-mutilation syndrome |
| fr | OBSOLETE : Maladie des brides amniotiques | |
| de | OBSOLET: Amnionruptur-Sequenz | OBSOLET: ADAM-Syndrom · OBSOLET: Amniotisches-Band-Syndrom |
| es | OBSOLETO: Bandas amnióticas | OBSOLETO: Síndrome ADAM · OBSOLETO: Síndrome de deformidad amniótica-adhesión-mutilación |
| it | OBSOLETO: Bande amniotiche | OBSOLETO: Sindrome ADAM · OBSOLETO: Sindrome deformità amniotica-adesione-mutilazione |
| nl | OBSOLEET: Amnionstrengen | OBSOLEET: ADAM-syndroom · OBSOLEET: Amnionmisvorming - adhesie - mutilatie-syndroom |
| pt | OBSOLETO: Bandas amnióticas | |
| pl | NIEAKTUALNE: Pasma owodniowe | NIEAKTUALNE: Zespół pasm owodniowych · NIEAKTUALNE: Zespół ADAM |
| cs | NEAKTUÁLNÍ: Amniální pruhy | NEAKTUÁLNÍ: ADAM syndrom · NEAKTUÁLNÍ: Syndrom zahrnující amniotické deformity, adhezi a mutilaci |
| uk | ЗАСТАРІЛО: Амніотичні перетяжки | ЗАСТАРІЛО: Синдром Адама · Синдром деформації амніотичної тканини, спайкового процесу та каліцтва |
| zh | 废弃：羊膜带 | 羊膜畸形-粘连-残缺综合征 |
| tr | Eski adı: Amniyotik bantlar | ADAM sendromu · Amniyotik deformite-adezyon-mutilasyon sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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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/1034
- This record as JSON: /data/d/1034.json