ORPHA:98979
Chandler syndrome
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
A clinical variant of iridocorneal endothelial (ICE) syndrome, characterized by very few iris abnormalities but more severe corneal edema and less severe secondary glaucoma than seen in the other two ICE syndrome variants: Cogan-Reese syndrome and essential iris atrophy.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Chandler syndrome | |
| fr | Syndrome de Chandler | |
| de | Chandler-Syndrom | |
| es | Síndrome de Chandler | |
| it | Sindrome di Chandler | |
| nl | Syndroom van Chandler | |
| pt | Síndrome Chandler | |
| pl | Zespół Chandlera | |
| cs | Chandlerův syndrom | |
| uk | Синдром Чандлера | |
| zh | Chandler综合征 | |
| tr | Chandler sendromu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H21.2 | NTBT | attributed | validated |
| ICD-11 | LA11.Y | NTBT | index | validated |
| MONDO | 0020369 | E | validated | |
| UMLS | C0544008 | E | validated | |
| GARD | 6033 | E | validated | |
| MedDRA | 10057487 | 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
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:64734Iridocorneal endothelial syndrome
rare developmental anomalies during embryogenesis; rare genetic diseases; rare ophthalmic disorders
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/98979
- This record as JSON: /data/d/98979.json