ORPHA:1804
Dyssegmental dysplasia-glaucoma syndrome
inactive · moved to ORPHA:156731Dyssegmental dysplasia, Rolland-Desbuquois type
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Dyssegmental dysplasia, Rolland-Desbuquois type
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Dyssegmental dysplasia-glaucoma syndrome | |
| fr | Syndrome de dysplasie dyssegmentaire-glaucome | |
| de | Dysplasie, dyssegmentale - Glaukom | |
| es | Síndrome de displasia disegmentaria-glaucoma | |
| it | Displasia dissegmentaria - glaucoma | |
| nl | Dyssegmentale dysplasie - glaucoom-syndroom | |
| pt | Síndrome de displasia dissegmentar-glaucoma | |
| pl | Dysplazja dyssegmentalna - jaskra | |
| cs | Syndrom zahrnující dyssegmentální dysplázii a glaukom | |
| uk | Синдром дисегментарної дисплазії-глаукоми | |
| zh | 节段性发育不良-青光眼综合征 | |
| tr | Dissegmental displazi-glokom sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 601561 | E | validated | |
| UMLS | C1832111 | 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/1804
- This record as JSON: /data/d/1804.json