Disease #05622 (AN1 (aniridia, type 1 (cataract with late-onset corneal dystrophy)), OMIM:106210)
| Official abbreviation |
AN1 |
| Name |
aniridia, type 1 (cataract with late-onset corneal dystrophy) |
| OMIM ID |
106210 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
PAX6 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2019-07-12 09:07:29 +02:00 (CEST) |
| Date last edited |
2023-12-23 15:14:09 +01:00 (CET) |
Individuals
|