raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:99723

OBSOLETE: Familial esophageal 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
LangNameSynonyms
enOBSOLETE: Familial esophageal achalasia
frOBSOLETE : Achalasie oesophagienne familiale
deOBSOLET: Familiäre oesophageale AchalasieOBSOLET: Ösophagus-Achalasie, familiäre
esOBSOLETO: Acalasia esofágica familiar
itOBSOLETO: Acalasia esofagea familiare
nlOBSOLEET: Familiale oesofageale achalasie
ptOBSOLETO: Acalasia, esofágica, familiar
plNIEAKTUALNE: Rodzinna achalazja przelyku
csNEAKTUÁLNÍ: Familiární achalázie jícnu
ukЗАСТАРІЛО: Сімейна ахалазія стравоходу
zh弃用:家族性食管失弛缓症
trEski adı: ailesel özofagus akalazyası
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card