raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:320317

OBSOLETE: Cleft lip/palate-ectodermal dysplasia syndrome

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

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 Cleft lip/palate-ectodermal dysplasia syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Cleft lip/palate-ectodermal dysplasia syndrome
frOBSOLETE : Syndrome de fente labiopalatine-dysplasie ectodermique
deOBSOLET: Lippen-Kiefer-Gaumenspalte - ektodermale DysplasieOBSOLET: CLEPD
esOBSOLETO: Síndrome de fisura labiopalatina-displasia ectodérmica
itOBSOLETO: Labio/palatoschisi - displasia ectodermicaOBSOLETO: CLEPD
nlOBSOLEET: Gespleten lip/verhemelte - ectodermale dysplasie-syndroom
ptOBSOLETO: Síndrome de fenda labial/palatina-displasia ectodérmica
plNIEAKTUALNE: Rozszczep wargi/podniebienia - dysplazja ektodermalnaNIEAKTUALNE: CLEPD
csNEAKTUÁLNÍ: Syndrom zahrnující rozštěp rtu/patra a ektodermální dyspláziiNEAKTUÁLNÍ: CLEPD
ukЗАСТАРІЛО: Синдром розщілини губи/піднебіння та ектодермальної дисплазії
zh弃用:唇裂外胚层发育不良综合征
trEski adı: Yarık dudak/damak-ektodermal displazi sendromu
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