raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:99987

OBSOLETE: Anophthalmia-esophageal-genital syndrome syndrome

inactive · referred to ORPHA:77298Anophthalmia/microphthalmia-esophageal atresia syndrome

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Anophthalmia/microphthalmia-esophageal atresia syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Anophthalmia-esophageal-genital syndrome syndrome
frOBSOLETE : Syndrome d'anophtalmie-syndrome oeso-génital
deOBSOLET: Anophthalmie-oesophageal-genitales-Syndrom
esOBSOLETO: Anoftalmia-síndrome esofágico-genital
itOBSOLETO: Anoftalmia - sindrome esofagea-genitale
nlOBSOLEET: Anoftalmie - oesofageaal-genitaal syndroom
ptOBSOLETO: Síndrome anoftalmia-esofágico-genital
plNIEAKTUALNE: Bezocze - zespól przelykowo-plciowy
csNEAKTUÁLNÍ: Syndrom zahrnující anoftalmii, ezofageální a genitální syndrom
ukЗАСТАРІЛО: Анофтальмо-стравохідно-генітальний синдром
zh弃用:眼炎-食道-生殖器综合征
trEski adı: Anoftalmi-özofagus-genital sendrom 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