raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1888

Ectrodactyly-ectodermal dysplasia without clefting syndrome

inactive · moved to ORPHA:1896EEC syndrome

Synonyms: EEC syndrome without cleft lip/palate

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 EEC syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enEctrodactyly-ectodermal dysplasia without clefting syndromeEEC syndrome without cleft lip/palate
frSyndrome d'ectrodactylie-dysplasie ectodermique sans fente labiopalatineEEC syndrome sans fente labiopalatine
deEktrodaktylie - ektodermale Dysplasie ohne Lippen-Kiefer-Gaumen-SpalteEEC-Syndrome ohne Lippen-Kiefer-Gaumen-Spalte
esSíndrome de ectrodactilia-displasia ectodérmica sin síndrome de hendidura
itEctrodattilia - displasia ectodermica senza labiopalatoschisiSindrome EEC senza labiopalatoschisi
nlEctrodactylie - ectodermale dysplasie zonder schisis-syndroomEEC-syndroom zonder gespleten lip/gehemelte
ptSíndrome de ectrodactilia-displasia ectodérmica sem fenda lábio-palatinaSíndrome EEC sem fenda lábio-palatina
plEktrodaktylia - dysplazja ektodermalna bez rozszczepianiaZespół EEC bez rozszczepu wargi/podniebienia
csSyndrom zahrnující ektrodaktylii a ektodermální dysplázii bez rozštěpuEEC syndrom bez rozštěpu rtu/patra
ukСиндром ектродактилії-ектодермальної дисплазії без розщепленняСиндром EEC без розщілини губи/піднебіння
zh缺指(趾)-外胚层发育不良不伴腭裂综合征无唇腭裂的EEC综合征
trEktrodaktili-kleft sendromu olmayan ektodermal displaziYarık dudak / damak olmayan EEC sendromu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM129810Evalidated
UMLSC1851849Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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