raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:206979

OBSOLETE: Granulomatous myositis

inactive · referred to ORPHA:98482Idiopathic inflammatory myopathy

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Idiopathic inflammatory myopathy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Granulomatous myositis
frOBSOLETE : Myosite granulomateuse
deOBSOLET: Myositis, granulomatöse
esOBSOLETO: Miositis granulomatosa
itOBSOLETO: Miosite granulomatosa
nlOBSOLEET: Granulomateuze myositis
ptOBSOLETO: Miosite granulomatosa
plNIEAKTUALNE: Ziarniniakowe zapalenie miesni
csNEAKTUÁLNÍ: Granulomatózní myozitida
ukЗАСТАРІЛО: Гранулематозний міозит
zh弃用:肉芽肿性肌炎
trEski adı: Granülomatöz miyozit
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