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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|