raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:86917

OBSOLETE: Lymphedema-cleft palate syndrome

inactive · referred to ORPHA:77240Primary lymphedema

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Primary lymphedema

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Lymphedema-cleft palate syndrome
frOBSOLETE : Syndrome de lymphoedme-fente palatine
deOBSOLET: Lymphödem - Gaumenspalte
esOBSOLETO: Síndrome de linfedema-fisura palatina
itOBSOLETO: Linfedema - palatoschisi
nlOBSOLEET: Lymfoedeem - gespleten verhemelte-syndroom
ptOBSOLETO: Síndrome de linfedema-fenda palatina
plNIEAKTUALNE: Obrzek limfatyczny - rozszczep podniebienia
csNEAKTUÁLNÍ: Syndrom lymfedému a rozštěpu patra
ukЗАСТАРІЛО: Синдром лімфедеми піднебіння з розщілиною піднебіння
zh弃用:淋巴水肿-腭裂综合征
trEski adı: Lenfödem-yarık damak 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