ORPHA:93442
Chondrodysplasia punctata
Synonyms: CDP
- 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 | Chondrodysplasia punctata | CDP |
| fr | Chondrodysplasie ponctuée | = en |
| de | Chondrodysplasia punctata | |
| es | Condrodisplasia punctata | |
| it | Condrodisplasia puntata | |
| nl | Chondrodysplasia punctata | = en |
| pt | Condrodisplasia pontuada | |
| pl | Chondrodysplazja punktowa | = en |
| cs | Chondrodysplasia punctata | CDP · Conradiho nemoc |
| uk | Хондродисплазія точкова | = en |
| zh | 点状软骨发育不良 | = en |
| tr | Kondrodisplazi punktata | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD24.04 | E | specific | validated |
| MONDO | 0019701 | E | validated | |
| MeSH | D002806 | E | validated | |
| UMLS | C0008445 | E | validated | |
| GARD | 8542 | E | validated | |
| MedDRA | 10087150 | 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/93442
- This record as JSON: /data/d/93442.json