Central serous chorioretinopathy
Synonyms: CSCR
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare, acquired, choroidal disorder characterized by subretinal detachment in the macular área and leakage of fluid under the retina that accumulates under the central macula. Symptoms tend to include blurred or distorted vision (metamorphopsia), moderate dyschromatopsia, relative central scotoma, hypermetropization, micropsia and reduced contrast sensitivity. A blurred or gray spot in the central visual field is common when the retina is detached.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Central serous chorioretinopathy | CSCR |
| fr | Choriorétinopathie séreuse centrale | CRSC |
| de | Zentrale seröse Chorioretinopathie | CCS · CSCR · Chorioretinopathia centralis serosa |
| es | Coriorretinopatía serosa central | = en |
| it | Corioretinopatia sierosa centrale | = en |
| nl | Centrale sereuze chorioretinopathie | = en |
| pt | Coriorretinopatia serosa central | |
| pl | Centralna chorioretinopatia surowicza | = en |
| cs | Centrální serózní chorioretinopatie | = en |
| uk | Центральна серозна хоріоретинопатія | = en |
| zh | 中心性浆液性脉络膜视网膜病变 | = en |
| tr | Santral seröz korioretinopati | = en |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H35.7 | NTBT | inclusion | validated |
| ICD-11 | 9B75.2 | E | specific | validated |
| MONDO | 0018616 | E | validated | |
| MeSH | D056833 | E | validated | |
| UMLS | C0730328 | E | validated | |
| GARD | 200 | E | validated | |
| MedDRA | 10086644 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:716348Rare isolated progressive predominantly chorioretinal disorder
rare ophthalmic disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/443079
- This record as JSON: /data/d/443079.json