raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:99872

OBSOLETE: Hashimoto-Pritzker syndrome

inactive · referred to ORPHA:389Langerhans cell histiocytosis

Synonyms: OBSOLETE: Congenital Langerhans cell histiocytosis

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 Langerhans cell histiocytosis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Hashimoto-Pritzker syndromeOBSOLETE: Congenital Langerhans cell histiocytosis
frOBSOLETE : Syndrome de Hashimoto-PritzkerOBSOLETE : Histiocytose langerhansienne congénitale
deOBSOLET: Hashimoto-Pritzker-SyndromOBSOLET: Langerhans-Zell-Histiozytose, kongenitale
esOBSOLETO: Síndrome de Hashimoto-PritzkerOBSOLETO: Histiocitosis congénita de células de Langerhans
itOBSOLETO: Sindrom di Hashimoto-PritzkerOBSOLETO: Istiocitosi congenita a cellule di Langerhans
nlOBSOLEET: Syndroom van Hashimoto-PritzkerOBSOLEET: Congenitale Langerhanscelhistiocytose
ptOBSOLETO: Síndrome Hashimoto-Pritzker
plNIEAKTUALNE: Zespól Hashimoto i PritzkeraNIEAKTUALNE: Wrodzona histiocytoza z komórek Langerhansa
csNEAKTUÁLNÍ: Hashimotova-Pritzkerova chorobaNEAKTUÁLNÍ: Vrozená Langerhansova histiocytóza X · NEAKTUÁLNÍ: Hashimoto-Pritzkerova choroba
ukЗАСТАРІЛО: Синдром Хашимото-ПріцкераЗАСТАРІЛО: Вроджений гістіоцитоз клітин Лангерганса
zh弃用:Hashimoto-Pritzker综合征先天性朗格汉斯细胞组织细胞增生症
trEski adı: Hashimoto-Pritzker sendromuDoğumsal Langerhans hücreli histiyositoz
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