raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:90318

OBSOLETE: Ehlers-Danlos syndrome type 2

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

Synonyms: OBSOLETE: EDS II

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