ORPHA:98567
Rare eyelid malposition disorder
Synonyms: Eyelids malposition disorder
- 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 | Rare eyelid malposition disorder | Eyelids malposition disorder |
| fr | Maladie rare de malposition de la paupière | Malposition du bord libre de la paupière |
| de | Augenlider, Fehlstellung der | |
| es | Trastorno por mala posición de los párpados | |
| it | Disturbo da malposizione delle palpebre | |
| nl | Ooglidmalpositiestoornis | |
| pt | Doença pálpebras mal posicionadas | |
| pl | Nieprawidłowe położenie powiek | = en |
| cs | Malpozice očních víček | = en |
| uk | Рідкісний розлад неправильного положення повік | Порушення положення повік |
| zh | 罕见眼睑错位症 | 眼睑错位症 |
| tr | Nadir görülen göz kapağı malpozisyon bozukluğu | Göz kapakları malpozisyon bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98560Rare palpebral disorder
rare developmental anomalies during embryogenesis; rare ophthalmic disorders
Children (11):
- ORPHA:1253Ascher syndrome
- ORPHA:99169Epiblepharon
- ORPHA:99172Euryblepharon
- ORPHA:519390Isolated blepharochalasis
- ORPHA:46486Mucous membrane pemphigoid
- ORPHA:519268Rare disorder with ectropion
- ORPHA:519270Rare disorder with entropion
- ORPHA:98578Rare disorder with ptosis
- ORPHA:98574Syndromic epicanthus
- ORPHA:98576Syndromic outer canthal malposition
- ORPHA:98575Syndromic telecanthus
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/98567
- This record as JSON: /data/d/98567.json