raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:206994

Bacterial myositis

Type
Disease
Group
Disorder
Age of onset
All ages
Status
active

A rare acquired skeletal muscle disease characterized by diffuse muscle infection without an intramuscular abscess. Although a wide variety of bacteria can be causative, the majority of cases are due to streptococcal infection. Signs and symptoms depend on the underlying infectious agent and include muscular pain, swelling, weakness, rash, acute rhabdomyolysis, myonecrosis, and gangrene.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enBacterial myositis
frMyosite bactérienne
deMyositis, bakterielle
esMiositis bacteriana
itMiosite batterica
nlBacteriële myositis
ptMiosite bacteriológica
plBakteryjne zapalenie mięśni
csBakteriální myozitida
ukБактеріальний міозит
zh细菌性肌炎
trBakteriyel miyozit

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10M60.0NTBTattributedvalidated
ICD-11FB30NTBTindexvalidated
MONDO0016127Evalidated
UMLSC0263979Evalidated
MedDRA10085526Evalidated

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