ORPHA:156005
Primary early-onset glaucoma
- 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 | Primary early-onset glaucoma | |
| fr | Glaucome à début précoce primitif | |
| de | Glaukom, primäres | |
| es | Glaucoma primario de inicio precoz | |
| it | Glaucoma primario | |
| nl | Primair glaucoom | |
| pt | Glaucoma primário de início precoce | |
| pl | Jaskra pierwotna | |
| cs | Primární glaukom | |
| uk | Первинна глаукома з раннім початком | |
| zh | 原发性早发性青光眼 | |
| tr | Primer erken-başlangıçlı glokom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15485 | E | validated | |
| UMLS | C5680656 | 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 (4):
- ORPHA:98553Developmental defect of the eye
rare developmental anomalies during embryogenesis - ORPHA:183557Genetic developmental defect of the eye
rare genetic diseases - ORPHA:523000Pediatric-onset glaucoma
rare ophthalmic disorders - ORPHA:359Pediatric-onset glaucoma of genetic origin
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/156005
- This record as JSON: /data/d/156005.json