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
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Congenital nasal pyriform aperture stenosis with holoprosencephaly | OBSOLETE: Apertura pyriformis with holoprosencephaly |
| fr | OBSOLETE : Syndrome de sténose congénitale des orifices piriformes-holoprosencéphalie | |
| de | OBSOLET: Kongenitale Stenose der Apertura piriformis mit Holoprosenzephalie | |
| es | OBSOLETO: Estenosis nasal congénita de la apertura piriforme con holoprosencefalia | OBSOLETO: Apertura piriforme con holoprosencefalia |
| it | OBSOLETO: Stenosi congenita degli orifizi piriformi nasali associata a oloprosencefalia | OBSOLETO: Orifizi piriformi associati a oloprosencefalia |
| nl | OBSOLEET: Congenitale nasale apertura piriformis stenose met holoprosencefalie | OBSOLEET: Apertura pyriformis met holoprosencefalie |
| pt | OBSOLETO: Estenose da abertura piriforme nasal congénita, com holoprosencefalia | |
| pl | NIEAKTUALNE: Wrodzone zwezenie otworu gruszkowego nosa z holoprozencefalia | NIEAKTUALNE: Otwór gruszkowy z holoprozencefalią |
| cs | NEAKTUÁLNÍ: Vrozená stenóza pyriformní apertury s holoprosencefalií | = en |
| uk | ЗАСТАРІЛО: Вроджений стеноз грушевидного отвору носу з голопрозенцефалією | ЗАСТАРІЛО: 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 |
| tr | Eski adı: Holoprozensefali ile seyreden doğumsal nazal piriform açıklık stenozu | Holoprozensefali ile seyreden apertura piriformis |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/162521
- This record as JSON: /data/d/162521.json