raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:172982

OBSOLETE: Congenital myopathy with fiber size variation

inactive · referred to ORPHA:97245Congenital 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 Congenital myopathy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Congenital myopathy with fiber size variation
frOBSOLETE : Myopathie congénitale avec taille de fibre variable
deOBSOLET: Kongenitale Myopathie mit Kalibervariationen der Muskelfasern
esOBSOLETO: Miopatía congénita con variación del tamaño de fibra
itOBSOLETO: Miopatia congenita con variazione delle dimensioni delle fibre
nlOBSOLEET: Congenitale myopathie met vezelgroottevariatie
ptOBSOLETO: Miopatia congénita com variação do tamanho das fibras
plNIEAKTUALNE: Wrodzona miopatia ze zmienna wielkoscia wlókien
csNEAKTUÁLNÍ: Myopatie s variabilitou velikosti svalových vláken
ukЗАСТАРІЛО: Вроджена міопатія з варіацією розміру волокон
zh弃用:先天性肌病伴纤维大小变异
trEski adı: Lif boyutu varyasyonlu doğumsal miyopati
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