raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93594

OBSOLETE: Alpha-1-antichymotrypsin deficiency

inactive · referred to ORPHA:447874Biological anomaly without phenotypic characterization

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Biological anomaly without phenotypic characterization

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Alpha-1-antichymotrypsin deficiency
frOBSOLETE : Déficit en alpha-1 antichymotrypsine
deOBSOLET: Alpha-1-Antichymotrypsin-Mangel
esOBSOLETO: Deficiencia de alfa-1-antiquimotripsina
itOBSOLETO: Deficit di alfa-1-antichimotripsina
nlOBSOLEET: Deficiëntie van alfa-1-antichymotrypsine
ptOBSOLETO: Deficiência de alfa-1-antiquimotripsina
plNIEAKTUALNE: Niedobór alfa-1-antychymotrypsyny
csNEAKTUÁLNÍ: Deficit alfa-1-antichymotrypsinu
ukЗАСТАРІЛО: Дефіцит альфа-1-антихімотрипсину
zh弃用:α-1-抗糜蛋白酶缺乏症
trEski adı: Alfa-1-antikimotripsin eksikliği
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