raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:90309

OBSOLETE: Ehlers-Danlos syndrome type 1

inactive · referred to ORPHA:287Classical Ehlers-Danlos syndrome

Synonyms: OBSOLETE: EDS I

Type
Etiological subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Classical Ehlers-Danlos syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Ehlers-Danlos syndrome type 1OBSOLETE: EDS I
frOBSOLETE : Syndrome d'Ehlers-Danlos type 1OBSOLETE : EDS I · OBSOLETE : SED I
deOBSOLET: Ehlers-Danlos-Syndrom Typ 1OBSOLET: EDS I
esOBSOLETO: Síndrome de Ehlers-Danlos tipo 1OBSOLETO: SED I
itOBSOLETO: Sindrome di Ehlers-Danlos, tipo 1= en
nlOBSOLEET: Syndroom van Ehlers-Danlos type 1OBSOLEET: EDS I
ptOBSOLETO: Síndrome Ehlers-Danlos tipo 1OBSOLETO: EDS I
plNIEAKTUALNE: Zespól Ehlersa i Danlosa typu 2 1NIEAKTUALNE: EDS I
csNEAKTUÁLNÍ: Ehlersův-Danlosův syndrom, typ 1NEAKTUÁLNÍ: EDS I · NEAKTUÁLNÍ: Ehlers-Danlosův syndrom, typ 1
ukЗАСТАРІЛО: Синдром Елерса-Данлоса, тип 1ЗАСТАРІЛО: EDS I
zh弃用:埃勒斯-当洛综合征1型EDSI型
trEski adı: Ehlers-Danlos sendromu tip 1EDS I
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