ORPHA:98697

OBSOLETE: Genetic keratinization disorder associated with ocular features

inactive · referred to ORPHA:281085Inherited ichthyosis syndromic form

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 Inherited ichthyosis syndromic form

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Genetic keratinization disorder associated with ocular features
fr	OBSOLETE : Trouble de la kératinisation avec atteintes oculaires
de	OBSOLET: Keratinisierungsstörung mit assoziierter Augenbeteiligung, genetisch bedingt
es	OBSOLETO: Trastorno genético de la queratinización asociado a manifestaciones oculares
it	OBSOLETO: Disturbo genetico della cheratinizzazione associato a segni oculari
nl	OBSOLEET: Genetische keratinisatiestoornis geassocieerd met oculaire kenmerken
pt	OBSOLETO: Doença da queratinização associada a doença ocular genética
pl	NIEAKTUALNE: Genetyczne zaburzenia rogowacenia z objawami ocznymi
cs	NEAKTUÁLNÍ: Geneticky podmíněné poruchy keratinizace s očními příznaky
uk	ЗАСТАРІЛО: Генетично обумовлене порушення кератинізації, повязане з особливостями очей
zh	弃用：遗传性角化异常相关性眼特征
tr	Eski adı: Oküler özelliklerle ilişkili genetik keratinizasyon bozukluğu

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/98697
This record as JSON: /data/d/98697.json