ORPHA:730322
Isolated anophthalmia
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Autosomal dominant, Autosomal recessive, X-linked recessive
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated anophthalmia | |
| fr | Anophtalmie isolée | |
| de | Anophthalmie, isolierte | |
| es | Anoftalmia aislada | |
| it | Anoftalmia isolata | |
| nl | Geïsoleerde anoftalmie | |
| pt | Isolated anophthalmia | |
| pl | Isolated anophthalmia | |
| cs | Isolated anophthalmia |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:2542Isolated microphthalmia-anophthalmia-coloboma
rare developmental anomalies during embryogenesis; rare genetic diseases; rare ophthalmic disorders
No children.
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/730322
- This record as JSON: /data/d/730322.json