raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:50817

Duane anomaly-myopathy-scoliosis syndrome

inactive · moved to ORPHA:2744Horizontal gaze palsy with progressive scoliosis

Synonyms: Verloes-Deprez syndrome

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Horizontal gaze palsy with progressive scoliosis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enDuane anomaly-myopathy-scoliosis syndromeVerloes-Deprez syndrome
frSyndrome d'anomalie de Duane-myopathie-scolioseSyndrome de Verloes-Deprez
deDuane-Anomalie-Myopathie-Skoliose-SyndromVerloes-Deprez-Syndrom
esSíndrome de anomalía de Duane-miopatía-escoliosisSíndrome de Verloes-Deprez
itAnomalia di Duane - miopatia - scoliosiSindrome di Verloes-Deprez
nlDuane-anomalie - myopathie - scoliose-syndroomSyndroom van Verloes-Deprez
ptSíndrome de anomalia Duane-miopatia-escolioseSíndrome Verloes-Deprez
plAnomalia Duane'a - miopatia- skoliozaZespół Verloesa i Depreza
csSyndrom zahrnující Duaneho anomálii, myopatii a skoliózuVerloesův-Deprezův syndrom · Verloes-Deprezův syndrom
ukСиндром аномалії Дуейна-міопатії-сколіозуСиндром Верлоеса-Депреса
zhDuane畸形-肌病-脊柱侧凸综合征Verloes-Deprez综合征
trDuane anomalisi-miyopati-skolyoz sendromuVerloes-Deprez sendromu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0033672Evalidated
UMLSC4302550Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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