ORPHA:98648
Musculoskeletal disease with cataract
- 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 | Musculoskeletal disease with cataract | |
| fr | Maladie musculo-squelettique avec cataracte | |
| de | Muskuloskelettale Krankheit mit Katarakt | |
| es | Enfermedad musculoesquelética con una posible catarata | |
| it | Cataratta associata a malattia muscoloscheletrica | |
| nl | Musculoskeletale ziekte met cataract | |
| pt | Doença musculoesquelética com catarata | |
| pl | Choroba mięśniowo-szkieletowa z zaćmą | |
| cs | Muskuloskeletální onemocnění s kataraktou | |
| uk | Захворювання опорно-рухового апарату з катарактою | |
| zh | 肌肉骨骼疾病伴白内障 | |
| tr | Katarakt ile seyreden kas-iskelet sistemi hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681664 | 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 (2):
- ORPHA:98641Syndromic cataract
rare ophthalmic disorders - ORPHA:522548Syndromic genetic cataract
rare genetic 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/98648
- This record as JSON: /data/d/98648.json