Disease #02487 (ASGD5 (dysgenesis, anterior segment, type 5, multiple subtypes), OMIM:604229)
| Official abbreviation |
ASGD5 |
| Name |
dysgenesis, anterior segment, type 5, multiple subtypes |
| OMIM ID |
604229 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
5 |
| Associated with 2 genes |
PAX6, PITX2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2025-11-26 23:05:16 +01:00 (CET) |
Individuals
|