ORPHA:251287
Benign concentric annular macular dystrophy
inactive · moved to ORPHA:791Retinitis pigmentosa
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Retinitis pigmentosa
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Benign concentric annular macular dystrophy | |
| fr | Dystrophie maculaire annulaire concentrique bénigne | |
| de | Makuladystrophie, anuläre benigne konzentrische | |
| es | Distrofia macular anular concéntrica benigna | |
| it | Distrofia maculare anulare concentrica benigna | |
| nl | Goedaardige concentrische annulaire maculadystrofie | Goedaardige concentrische ringvormige maculadystrofie |
| pt | Distrofia macular anular concêntrica benigna | |
| pl | Łagodna koncentryczna pierścieniowa dystrofia plamki | |
| cs | Benigní koncentrická anulární makulární dystrofie | |
| uk | Доброякісна концентрична кільцева макулодистрофія | |
| zh | 良性同心环状黄斑营养不良 | |
| tr | Selim eşmerkezli anüler maküler distrofi |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H31.8 | NTBT | attributed | validated |
| ICD-11 | 9B75.Y | NTBT | index | validated |
| MONDO | 0007934 | E | validated | |
| UMLS | C4304667 | E | validated | |
| GARD | 9887 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/251287
- This record as JSON: /data/d/251287.json