Disease #00153 (AVSD (septal defect, atrioventricular (AVSD)), OMIM:606215)
| Official abbreviation |
AVSD |
| Name |
septal defect, atrioventricular (AVSD) |
| OMIM ID |
606215 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
39 |
| Phenotype entries for this disease |
37 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-06-19 09:52:14 +02:00 (CEST) |
| Date last edited |
2015-12-08 23:54:35 +01:00 (CET) |
Individuals
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