raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:206638

Acquired skeletal muscle disease

Type
Category
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAcquired skeletal muscle disease
frMaladie acquise du muscle squelettique
deErworbene Krankheit der Skelettmuskeln
esEnfermedad muscular esquelética adquirida
itMalattia acquisita del muscolo scheletrico
nlVerworven skeletspierziekte
ptDoença do músculo esquelético adquirida
plNabyta choroba mięśni szkieletowych
csZískaná muskuloskeletální onemocnění
ukНабуті захворювання скелетних мязів
zh获得性骨骼肌病
trEdinsel iskelet kası hastalığı
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016105Evalidated
MONDO16105Evalidated
UMLSC5680799Evalidated

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):

Children (7):

Codes that Orphanet moved or referred to this one:

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