ORPHA:519329
Rare disorder involving multiple structures of the eye
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare disorder involving multiple structures of the eye | |
| fr | Maladie rare avec atteinte de multiples structures de l'oeil | |
| de | Seltene Krankheit mit Beteiligung multipler Strukturen des Auges | |
| es | Trastorno raro con afectación de múltiples estructuras del ojo | |
| it | Malattia rara coinvolgente strutture oculari multiple | |
| nl | Zeldzame stoornis met betrokkenheid van multipele oogstructuren | |
| pt | Doença rara com envolvimento de múltiplas estruturas oculares | |
| pl | Rzadka choroba obejmująca liczne struktury gałki ocznej | |
| cs | Vzácná porucha zahrnující více očních struktur | |
| uk | Рідкісне захворювання, що охоплює кілька структур ока | |
| zh | 罕见累及眼部多个结构的病变 | |
| tr | Gözün birden çok yapısını içeren nadir bozukluk |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681352 | 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:520814Rare disorder of the visual organs
rare ophthalmic disorders
Children (13):
- ORPHA:617449Congenital aphakia-iris hypoplasia-microphthalmia-microcornea syndrome
- ORPHA:141132Craniofacial microsomia
- ORPHA:199323Endophthalmitis
- ORPHA:466682Euthyroid Graves orbitopathy
- ORPHA:314555Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome
- ORPHA:636950Glaucomatocyclitic crisis disease
- ORPHA:728633Idiopathic orbital inflammation syndrome
- ORPHA:449563IgG4-related ophthalmic disease
- ORPHA:647815Keratitis fugax hereditaria
- ORPHA:98706Oculocutaneous or ocular albinism
- ORPHA:523000Pediatric-onset glaucoma
- ORPHA:1214Progressive hemifacial atrophy
- ORPHA:90080Scarring in glaucoma filtration surgical procedures
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/519329
- This record as JSON: /data/d/519329.json