Disease #01180 (ASGD1 (dysgenesis, anterior segment, type 1), OMIM:107250)
| Official abbreviation |
ASGD1 |
| Name |
dysgenesis, anterior segment, type 1 |
| OMIM ID |
107250 |
| 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 |
PITX3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2025-11-10 16:35:46 +01:00 (CET) |
Individuals
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