Disease #01344 (ASGD4 (dysgenesis, anterior segment, type 4), OMIM:137600)
| Official abbreviation |
ASGD4 |
| Name |
dysgenesis, anterior segment, type 4 |
| OMIM ID |
137600 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PITX2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2025-11-26 22:58:24 +01:00 (CET) |
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