ORPHA:98658
Color-vision disease
- 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 | Color-vision disease | |
| fr | Trouble de la vision des couleurs | |
| de | Farbsehstörung | |
| es | Enfermedad de la visión de los colores | |
| it | Malattia della visione a colori | |
| nl | Kleurwaarnemingsziekte | |
| pt | Doença da visão cromática | |
| pl | Choroba rozróżniania kolorów | |
| cs | Poruchy barevného vidění | |
| uk | Захворювання кольорового зору | |
| zh | 颜色-视觉疾病 | |
| tr | Renk körlüğü hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H53.5 | E | specific | validated |
| MONDO | 0001703 | E | validated | |
| MONDO | 1703 | E | validated | |
| UMLS | C5681659 | 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:101435Rare genetic eye disease
rare genetic diseases - ORPHA:97966Rare ophthalmic disorder
rare ophthalmic disorders
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/98658
- This record as JSON: /data/d/98658.json