ORPHA:93452
OBSOLETE: Craniosynostosis syndrome or cranial ossification disease
inactive · referred to ORPHA:139393Syndromic craniosynostosis
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Syndromic craniosynostosis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Craniosynostosis syndrome or cranial ossification disease | |
| fr | OBSOLETE : Craniosténose ou anomalie de l'ossification crânienne | |
| de | OBSOLET: Kraniosynostose-Syndrom und kraniale Verknöcherung | |
| es | OBSOLETO: Síndrome de craneosinostosis o enfermedad de la osificación craneal | |
| it | OBSOLETO: Sindrome da craniosinostosi e malattia dell'ossificazione cranica | |
| nl | OBSOLEET: Craniosynostosesyndroom van craniale ossificatieziekte | |
| pt | OBSOLETO: Síndrome craniossinostose e doença da ossificação craniana | |
| pl | NIEAKTUALNE: Zespól kraniosynostozy lub zaburzenia kostnienia czaszki | |
| cs | NEAKTUÁLNÍ: Syndrom kraniosynostózy nebo onemocnění osifikace lebky | |
| uk | ЗАСТАРІЛО: Синдром краніосиностозу або хвороба окостеніння черепа | |
| zh | 弃用:颅缝早闭综合征或颅缝骨化症 | |
| tr | Eski adı: Kraniosinostozis sendromu veya kraniyal ossifikasyon hastalığı |
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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/93452
- This record as JSON: /data/d/93452.json