ORPHA:93465
Lethal chondrodysplasia
- Type
- Category
- 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 | Lethal chondrodysplasia | |
| fr | Chondrodysplasie létale | |
| de | Chondrodysplasie, letale | |
| es | Condrodisplasia letal | |
| it | Condrodisplasia letale | |
| nl | Letale chondrodysplasie | |
| pt | Condrodisplasia letal | |
| pl | Chondrodysplazja śmiertelna | |
| cs | Letální chondrodysplázie | |
| uk | Летальна хондродисплазія | |
| zh | 致死性软骨发育不全 | |
| tr | Letal kondrodisplazi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681594 | 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
Codes that Orphanet moved or referred to this one:
- ORPHA:1420OBSOLETE: Lethal chondrodysplasia, Moerman type referred to · inactive
- ORPHA:1421OBSOLETE: Lethal chondrodysplasia, Seller type referred to · inactive
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/93465
- This record as JSON: /data/d/93465.json