ORPHA:519339
Pseudopapilledema
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pseudopapilledema | |
| fr | Pseudo-oedème papillaire | |
| de | Pseudopapillenödem | |
| es | Pseudopapiledema | |
| it | Pseudopapilledema | |
| nl | Pseudopapiloedeem | |
| pt | Pseudopapiledema | |
| pl | Pseudoobrzęk tarczy nerwu wzrokowego | |
| cs | Pseudoedém papily | |
| uk | Псевдопапілома | |
| zh | 假视神经乳头水肿 | |
| tr | Psödopapilödem |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 8331 | E | validated | |
| MeSH | C562401 | E | validated | |
| UMLS | C0155300 | E | validated | |
| MedDRA | 10037141 | 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 (2):
- ORPHA:522512Rare genetic optic nerve disorder
rare genetic diseases - ORPHA:519351Rare optic nerve disorder
rare ophthalmic disorders
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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/519339
- This record as JSON: /data/d/519339.json