ORPHA:620152
Non-syndromic multisutural craniosynostosis
Synonyms: Isolated multisutural craniosynostosis · Non-syndromic multiple suture synostosis
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
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.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-syndromic multisutural craniosynostosis | Isolated multisutural craniosynostosis · Non-syndromic multiple suture synostosis |
| fr | Craniosynostose multisuturaire non syndromique | Craniosynostose multisuturaire isolée |
| de | Kraniosynostose, multisuturale, nicht-syndromale | Isolierte multisuturale Kraniosynostose · Multiple Nahtsynostose, nicht-syndromale |
| es | Craneosinostosis multisutural no sindrómica | Craneosinostosis multisutural aislada · Sinostosis de sutura múltiple no sindrómica |
| it | Craniosinostosi multisuturale non sindromica | Craniosinostosi isolata multisuturale · Sinostosi di diverse suture non sindromica |
| nl | Niet-syndromale multisuturale craniosynostose | Geïsoleerde multisuturale craniosynostose · Niet-syndromale synostose van meerdere schedelnaden |
| pt | Craniossinostose multissutural não-sindromática | Craniossinostose multissutural isolada · Sinostose de múltiplas suturas não-sindromática |
| pl | Niesyndromiczna kraniosynostoza obejmująca wiele szwów | = en |
| cs | Nesyndromická multisuturální kraniosynostóza | = en |
| uk | Несиндромальний краніосиностоз декількох швів | Ізольований мультисуглобовий краніосиностоз · Несиндромний множинний шовний синостоз |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0850077 | E | validated | |
| UMLS | C5680397 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:139390Non-syndromic craniosynostosis
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases
Children (9):
- ORPHA:620198Non-syndromic bicoronal and metopic craniosynostosis
- ORPHA:620205Non-syndromic bicoronal and sagittal craniosynostosis
- ORPHA:35099Non-syndromic bicoronal craniosynostosis
- ORPHA:1516Non-syndromic bilambdoid and sagittal craniosynostosis
- ORPHA:620178Non-syndromic bilambdoid craniosynostosis
- ORPHA:620192Non-syndromic metopic and sagittal craniosynostosis
- ORPHA:620158Non-syndromic non-specific multisutural craniosynostosis
- ORPHA:620212Non-syndromic pansynostosis
- ORPHA:620186Non-syndromic unicoronal and sagittal craniosynostosis
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/620152
- This record as JSON: /data/d/620152.json