raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98702

OBSOLETE: Connective tissue disease with eye involvement

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Connective tissue disease with eye involvement
frOBSOLETE : Maladie du tissu conjonctif avec atteinte ophtalmologique
deOBSOLET: Bindegewebskrankheit mit Augenbeteiligung
esOBSOLETO: Enfermedad del tejido conectivo con afectación ocular
itOBSOLETO: Malattia del tessuto connettivo, associata a malattia oculare
nlOBSOLEET: Bindweefselziekte met betrokkenheid van oog
ptOBSOLETO: Doença do tecido conjuntivo com envolvimento ocular
plNIEAKTUALNE: Choroba tkanki lacznej obejmujaca oko
csNEAKTUÁLNÍ: Onemocnění pojivové tkáně s postižením očí
ukЗАСТАРІЛО: Захворювання сполучної тканини з ураженням очей
zh弃用:结缔组织病伴眼受累
trEski adı: Göz tutulumu ile seyreden bağ dokusu hastalığı
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