Disease #05505 (ASD1 (septal defect, atrial, type 1, primum type (ASD1)), OMIM:108800)
| Official abbreviation |
ASD1 |
| Name |
septal defect, atrial, type 1, primum type (ASD1) |
| OMIM ID |
108800 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2018-11-08 16:10:34 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|