raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:90338

Margarita island ectodermal dysplasia

inactive · moved to ORPHA:3253Cleft lip/palate-ectodermal dysplasia syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Cleft lip/palate-ectodermal dysplasia syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enMargarita island ectodermal dysplasia
frDysplasie ectodermique type île Margarita
deDysplasie, ektodermale, Typ Margarita Island
esDisplasia ectodérmica tipo isla Margarita
itDisplasia ectodermica dell'isola Margarita
nlMargarita eiland ectodermale dysplasie
ptDisplasia ectodérmica tipo ilha Margarita
plDysplazja ektodermalna wyspy Margarita
csEktodermální dysplázie ostrova Margarita
ukЕктодермальна дисплазія острова Маргарити
zh玛格丽特岛外胚层发育不良
trMargarita adası ektodermal displazisi
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