ORPHA:98655
Lens shape anomaly
- 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 | Lens shape anomaly | |
| fr | Anomalie de forme du cristallin | |
| de | Linsenanomalie (Form) | |
| es | Anomalía en la forma de las lentes | |
| it | Anomalia della forma del cristallino | |
| nl | Lensvormanomalie | |
| pt | Anomalia da forma do cristalino | |
| pl | Nieprawidłowy kształt soczewki | |
| cs | Anomálie tvaru čočky | |
| uk | Аномалія форми кришталика | |
| zh | 晶状体形状异常 | |
| tr | Lens şekli anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C0158553 | 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 (4):
- ORPHA:98553Developmental defect of the eye
rare developmental anomalies during embryogenesis - ORPHA:183557Genetic developmental defect of the eye
rare genetic diseases - ORPHA:183607Genetic lens and zonula anomaly
rare genetic diseases - ORPHA:98639Rare lens disease
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98655
- This record as JSON: /data/d/98655.json