ORPHA:98980
Cogan-Reese syndrome
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
A clinical variant of iridocorneal endothelial (ICE) syndrome, characterized by variable iris atrophy, pigmented and pedunculated nodules on the iris and corneal abonormalities. Secondary glaucoma is also a common complication of the disease.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cogan-Reese syndrome | |
| fr | Syndrome de Cogan-Reese | |
| de | Cogan-Reese-Syndrom | |
| es | Síndrome de Cogan-Reese | |
| it | Sindrome di Cogan-Reese | |
| nl | Syndroom van Cogan-Reese | |
| pt | Síndrome Cogan-Reese | |
| pl | Zespół Cogana i Reese'a | |
| cs | Coganův-Reeseho syndrom | Cogan-Reeseho syndrom |
| uk | Синдром Когана-Різа | |
| zh | Cogan-Reese综合征 | |
| tr | Cogan-Reese sendromu |
Definition in:
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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 | 0020370 | E | validated | |
| UMLS | C1168173 | E | validated | |
| GARD | 6125 | E | validated | |
| MedDRA | 10059200 | 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/98980
- This record as JSON: /data/d/98980.json