raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2543

OBSOLETE: Microphthalmia-cataract syndrome

inactive · referred to ORPHA:2542Isolated microphthalmia-anophthalmia-coloboma

Synonyms: OBSOLETE: Congenital cataract-microphthalmia syndrome

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 Isolated microphthalmia-anophthalmia-coloboma

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Microphthalmia-cataract syndromeOBSOLETE: Congenital cataract-microphthalmia syndrome
frOBSOLETE : Syndrome de microphtalmie-cataracteOBSOLETE : Cataracte congénitale avec microphtalmie
deOBSOLET: Mikrophthalmie-Katarakt-Syndrom
esOBSOLETO: Síndrome de microftalmia-catarataOBSOLETO: Síndrome congénito de catarata-microftalmia
itOBSOLETO: Sindrome cicroftalmia-catarattaOBSOLETO: Sindrome cataratta congenita-microftalmia
nlOBSOLEET: Microftalmie - cataract-syndroomOBSOLEET: Congenitaal cataract - microftalmie-syndroom
ptOBSOLETO: Síndrome de microftalmia-catarataOBSOLETO: Catarata congénita com microftalmia
plNIEAKTUALNE: Maloocze - zacmaNIEAKTUALNE: Zaćma wrodzona - małoocze
csNEAKTUÁLNÍ: Syndrom mikroftalmie a katarakty= en
ukЗАСТАРІЛО: Синдром мікрофтальмії-катарактиЗАСТАРІЛО: Синдром вродженої катаракти-мікрофтальмії
zh弃用:小眼畸形-白内障综合征先天性白内障-小眼畸形综合征
trEski adı: Mikroftalmi-katarakt sendromuDoğumsal katarakt-mikroftalmi 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