anterior segment dysgenesis
Information
- Disease name
- anterior segment dysgenesis
- Disease ID
- DOID:0060648
- Description
- "An eye disease that is characterized by iris hypoplasia, an enlarged or reduced corneal diameter, corneal vascularization and opacity, posterior embryotoxon, corectopia, polycoria, an abnormal iridocorneal angle, ectopia lentis, and anterior synechiae between the iris and posterior corneal surface and is located_in the anterior segment of the eye." [url:https\://rarediseases.info.nih.gov/diseases/10025/anterior-segment-dysgenesis, url:https\://www.ncbi.nlm.nih.gov/pubmed/17914436, url:https\://www.ncbi.nlm.nih.gov/pubmed/30242500]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:5614
- Cross Reference ID (Disease Ontology)
- GARD:10025
- Cross Reference ID (Disease Ontology)
- ICD10CM:Q13.8
- Cross Reference ID (Disease Ontology)
- MIM:PS107250
- Cross Reference ID (Disease Ontology)
- ORDO:88632
- Exact Synonym (Disease Ontology)
- anterior segment developmental anomaly
- Exact Synonym (Disease Ontology)
- corneal opacification and other ocular anomalies
- Exact Synonym (Disease Ontology)
- sclerocornea with other ocular anomalies
- OMIM Phenotype Series Number (OMIM)
- PS107250