ORPHA:93443
Neonatal osteosclerotic dysplasia
- 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
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Neonatal osteosclerotic dysplasia | |
| fr | Ostéosclérose néonatale | |
| de | Dysplasie, neonatale osteosklerotische | |
| es | Displasia osteosclerótica neonatal | |
| it | Displasia osteosclerotica neonatale | |
| nl | Neonatale osteosclerotische dysplasie | |
| pt | Displasia osteosclerótica neonatal | |
| pl | Dysplazja osteosklerotyczna noworodków | |
| cs | Novorozenecké osteosklerotické dysplázie | |
| uk | Неонатальна остеосклеротична дисплазія | |
| zh | 新生儿骨硬化性发育不良 | |
| tr | Yenidoğan osteosklerotik displazi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019702 | E | validated | |
| UMLS | C1300205 | 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:93444Primary bone dysplasia with increased bone density
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases
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/93443
- This record as JSON: /data/d/93443.json