raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:99990

Brill-Zinsser disease

Synonyms: Brill disease · Recrudescent typhus

Type
Clinical subtype
Group
Subtype of disorder
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enBrill-Zinsser diseaseBrill disease · Recrudescent typhus
frMaladie de Brill-ZinsserMaladie de Brill · Typhus résurgent
deBrill-Zinsser-KrankheitBrill-Krankheit
esEnfermedad de Brill-ZinsserSíndrome de Brill · Tifus recrudescente
itMalattia di Brill-ZinsserMalattia di Brill · Tifo ricorrente
nlZiekte van Brill-ZinsserOpflakkering van tyfus · Ziekte van Brill
ptDoença de Brill-Zinsser
plChoroba Brilla i ZinsseraChoroba Brilla · Dur wysypkowy nawrotowy
csBrillova-Zinsserova nemocBrillova nemoc · Tyfus epidemický přenášený vešmi · Brill-Zinsserova nemoc
ukХвороба Бриля-ЦинссераХвороба Брілла · Рецидивний висипний тиф
zhBrill-Zinsser病复发性斑疹伤寒
trBrill-Zinsser hastalığıBrill hastalığı · Tekrarlayan tifüs
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10A75.1Especificvalidated
ICD-111C30.1Especificvalidated
MONDO0005680Evalidated
UMLSC0006181Evalidated
MedDRA10038017Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

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