Disease #01180 (ASGD1 (dysgenesis, anterior segment, type 1 (ASGD1)), OMIM:107250)
| Official abbreviation |
ASGD1 |
| Name |
dysgenesis, anterior segment, type 1 (ASGD1) |
| OMIM ID |
107250 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 2 genes |
FOXE3, PITX3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|