ORPHA:636950
Glaucomatocyclitic crisis disease
Synonyms: Posner-Schlossman syndrome
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Glaucomatocyclitic crisis disease | Posner-Schlossman syndrome |
| fr | Maladie à crises glaucomatocyclitiques | Syndrome de Posner-Schlossman |
| de | Posner-Schlossmann-Syndrom | Glaukomatozyklische Krise |
| es | Enfermedad de crisis glaucomatociclíticas | Síndrome de Posner-Schlossman |
| it | Malattia della crisi glaucomatociclitica | Sindrome di Posner-Schlossman |
| nl | Glaucomatocyclitische crisis-ziekte | Syndroom van Posner-Schlossman |
| pt | Doença glaucomatociclítica por crises | Síndrome Posner-Schlossman |
| pl | Przełom jaksrowo-rzęskowy | = en |
| cs | Onemocnění s glaukomatocyklitickými krizemi | = en |
| uk | Глаукоматоциклічна кризова хвороба | Синдром Познера-Шлоссмана |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H40.4 | NTBT | index | validated |
| ICD-11 | 9C61.24 | NTBT | attributed | validated |
| MONDO | 0004772 | E | validated | |
| UMLS | C0152138 | 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 (1):
- ORPHA:519329Rare disorder involving multiple structures of the eye
rare ophthalmic disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Europe | Class only | Validated | 35015437[PMID]_ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/636950
- This record as JSON: /data/d/636950.json