raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:206991

Viral myositis

Type
Disease
Group
Disorder
Age of onset
All ages
Status
active

A rare acquired skeletal muscle disease characterized by sudden onset of muscle weakness, tenderness, and pain during or following recovery from a viral illness. The most commonly reported underlying viral infections are influenza B and A, the latter being the significantly less frequent cause. Most cases occur in children. Symptoms are often limited to the calf muscles, but other muscle groups may be involved as well. The condition is typically self-limiting, resolving within several days, although rhabdomyolysis with renal failure and compartment syndrome have been reported.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enViral myositis
frMyosite virale
deMyositis, virale
esMiositis viral
itMiosite virale
nlVirale myositis
ptMiosite viral
plWirusowe zapalenie mięśni
csVirová myozitida
ukВірусний міозит
zh病毒性肌炎
trViral miyozit

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10M60.0NTBTattributedvalidated
ICD-11FB30NTBTindexvalidated
MONDO0016126Evalidated
UMLSC0150005Evalidated
MedDRA10051512Evalidated

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