ORPHA:98709

OBSOLETE: Ectodermal malformation syndrome associated with ocular features

inactive · referred to ORPHA:520814Rare disorder of the visual organs

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 Rare disorder of the visual organs

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Ectodermal malformation syndrome associated with ocular features
fr	OBSOLETE : Dysplasie ectodermique avec atteintes oculaires
de	OBSOLET: Ektodermales Fehlbildungssyndrom mit assoziierter Augenbeteiligung
es	OBSOLETO: Síndrome de malformación ectodérmica asociado a manifestaciones oculares
it	OBSOLETO: Sindrome malformativa ectodermica associata a segni oculari
nl	OBSOLEET: Ectodermaal malformatiesyndroom geassocieerd met oculaire kenmerken
pt	OBSOLETO: Síndrome de malformação ectodérmica com doença ocular
pl	NIEAKTUALNE: Zespól zaburzen ektodermalnych zwiazany z objawami ocznymi
cs	NEAKTUÁLNÍ: Syndromy s ektodermální malformací asociované s očními příznaky
uk	ЗАСТАРІЛО: Синдром ектодермальних вад розвитку, повязаний з очними особливостями
zh	弃用：外胚叶畸形综合征相关性眼特征
tr	Eski adı: Oküler özellikler ile seyreden ektodermal malformasyon sendromu

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Not placed in any Orphanet classification in this release.

No children.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/98709
This record as JSON: /data/d/98709.json