ORPHA:99722
OBSOLETE: Sporadic achalasia
inactive · referred to ORPHA:930Idiopathic achalasia
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Idiopathic achalasia
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Sporadic achalasia | |
| fr | OBSOLETE : Achalasie sporadique | |
| de | OBSOLET: Achalasie, sporadische | |
| es | OBSOLETO: Acalasia, forma esporádica | |
| it | OBSOLETO: Acalasia, forma sporadica | |
| nl | OBSOLEET: Sporadische achalasie | |
| pt | OBSOLETO: Acalasia esporádica | |
| pl | NIEAKTUALNE: Achalazja sporadyczna | |
| cs | NEAKTUÁLNÍ: Sporadická achalázie | |
| uk | ЗАСТАРІЛО: Спорадична ахалазія | |
| zh | 弃用：散发性食管失弛缓症 | |
| tr | Eski adı: Sporadik akalazya |
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/99722
- This record as JSON: /data/d/99722.json