raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:162521

OBSOLETE: Congenital nasal pyriform aperture stenosis with holoprosencephaly

inactive · referred to ORPHA:280200Microform holoprosencephaly

Synonyms: OBSOLETE: Apertura pyriformis with holoprosencephaly

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 Microform holoprosencephaly

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Congenital nasal pyriform aperture stenosis with holoprosencephalyOBSOLETE: Apertura pyriformis with holoprosencephaly
frOBSOLETE : Syndrome de sténose congénitale des orifices piriformes-holoprosencéphalie
deOBSOLET: Kongenitale Stenose der Apertura piriformis mit Holoprosenzephalie
esOBSOLETO: Estenosis nasal congénita de la apertura piriforme con holoprosencefaliaOBSOLETO: Apertura piriforme con holoprosencefalia
itOBSOLETO: Stenosi congenita degli orifizi piriformi nasali associata a oloprosencefaliaOBSOLETO: Orifizi piriformi associati a oloprosencefalia
nlOBSOLEET: Congenitale nasale apertura piriformis stenose met holoprosencefalieOBSOLEET: Apertura pyriformis met holoprosencefalie
ptOBSOLETO: Estenose da abertura piriforme nasal congénita, com holoprosencefalia
plNIEAKTUALNE: Wrodzone zwezenie otworu gruszkowego nosa z holoprozencefaliaNIEAKTUALNE: Otwór gruszkowy z holoprozencefalią
csNEAKTUÁLNÍ: Vrozená stenóza pyriformní apertury s holoprosencefalií= en
ukЗАСТАРІЛО: Вроджений стеноз грушевидного отвору носу з голопрозенцефалієюЗАСТАРІЛО: Пірамідальна апертура з голопрозенцефалією
zh弃用:先天性鼻梨状窝狭窄伴前脑无裂畸形梨状孔伴前脑全裂
trEski adı: Holoprozensefali ile seyreden doğumsal nazal piriform açıklık stenozuHoloprozensefali ile seyreden apertura piriformis
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