raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2535

OBSOLETE: Microcornea-corectopia-macular hypoplasia syndrome

inactive · referred to ORPHA:519286Rare disorder of the pupil

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 Rare disorder of the pupil

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Microcornea-corectopia-macular hypoplasia syndrome
frOBSOLETE : Syndrome de microcornée-corectopie-hypoplasie maculaire
deOBSOLET: Mikrokornea-Korektopie-Makulahypoplasie-Syndrom
esOBSOLETO: Síndrome de microcórnea-corectopia-hipoplasia macular
itOBSOLETO: Microcornea - ectopia della coroide - ipoplasia maculare
nlOBSOLEET: Microcornea - corectopie - maculahypoplasie-syndroom
ptOBSOLETO: Síndrome microcórnea-corectopia-hipoplasia da mácula
plNIEAKTUALNE: Rogówka mala - przemieszczenie zrenicy - hipoplazja plamki
csNEAKTUÁLNÍ: Syndrom zahrnující mirkokorneu, korektopii a makulární hypoplázii
ukСиндром мікрокорнеа-коректопії-макулярної гіпоплазії
zh弃用:小角膜-瞳孔异位-黄斑发育不全综合征
trEski adı: Mikrokornea-korektopi-maküler hipoplazi 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