ORPHA:284804
Ocular albinism
- 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 | Ocular albinism | |
| fr | Albinisme oculaire | |
| de | Albinismus, okulärer | |
| es | Albinismo ocular | |
| it | Albinismo oculare | |
| nl | Oculair albinisme | |
| pt | Albinismo ocular | |
| pl | Albinizm oczny | |
| cs | Oční albinismus | Okulární albinismus |
| uk | Очний альбінізм | |
| zh | 眼白化病 | |
| tr | Oküler albinizm |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 9E1Y | NTBT | index | validated |
| MONDO | 0017304 | E | validated | |
| MONDO | 17304 | E | validated | |
| MeSH | D016117 | E | validated | |
| UMLS | C0078917 | E | validated | |
| MedDRA | 10065276 | 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:352728Disorder of melanin metabolism
rare inborn errors of metabolism; rare genetic diseases - ORPHA:98706Oculocutaneous or ocular albinism
rare genetic diseases; 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/284804
- This record as JSON: /data/d/284804.json