ORPHA:93437
Acromesomelic 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 | Acromesomelic dysplasia | |
| fr | Dysplasie acromésomélique | |
| de | Dysplasie, akromesomele | |
| es | Displasia acromesomélica | |
| it | Displasia acromesomelica | |
| nl | Acromesomele dysplasie | |
| pt | Displasia acromesomélica | |
| pl | Dysplazja akromezomeliczna | |
| cs | Akromezomelické dysplázie | |
| uk | Акромезотеліальна дисплазія | |
| zh | 肢端肢中发育不全 | |
| tr | Akromezomelik displazi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD24.9 | E | specific | validated |
| MONDO | 0019696 | E | validated | |
| MeSH | C535658 | E | validated | |
| UMLS | C5235036 | E | validated | |
| GARD | 6 | E | validated | |
| MedDRA | 10083866 | 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:364526Primary bone dysplasia
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/93437
- This record as JSON: /data/d/93437.json