raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:275534

OBSOLETE: Myostatin-related muscle hypertrophy

inactive · referred to ORPHA:98053Rare genetic disease

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare genetic disease

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Myostatin-related muscle hypertrophy
frOBSOLETE : Hypertrophie musculaire liée à la myostatine
deOBSOLET: Muskelhypertrophie, Myostatin-abhängige
esOBSOLETO: Hipertrofia muscular asociada a la miostatina
itOBSOLETO: Ipertrofia muscolare associata alla miostatina
nlOBSOLEET: Myostatinegerelateerde spierhypertrofie
ptOBSOLETO: Hipertrofia muscular miostatina-relacionada
plNIEAKTUALNE: Hipertrofia mięśniowa związana z miostatynąNIEAKTUALNE: Przerost mięśni związany z miostatyną
csNEAKTUÁLNÍ: Svalová hypertrofie související s myostatinem
ukЗАСТАРІЛО: Міостатинова гіпертрофія мязів
zh肌肉生长抑制素相关肌肉肥大
trMiyostatin -ilişkili kas hipertrofisi
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