raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:207003

OBSOLETE: Endocrine myopathy

inactive · referred to ORPHA:206638Acquired skeletal muscle disease

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 Acquired skeletal muscle disease

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Endocrine myopathy
frOBSOLETE : Myopathie endocrinienne
deOBSOLET: Myopathie, endokrine
esOBSOLETO: Miopatía endocrina
itOBSOLETO: Miopatia endocrina
nlOBSOLEET: Endocriene myopathie
ptOBSOLETO: Miopatia endócrina
plNIEAKTUALNE: Endokrynowe zapalenie miesni
csNEAKTUÁLNÍ: Endokrinní myopatie
ukЗАСТАРІЛО: Ендокринна міопатія
zh弃用:内分泌性肌病
trEski adı: Endokrin 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