Disease #00137 (AOS1 (Adams-Oliver syndrome, type 1 (AOS1)), OMIM:100300)
| Official abbreviation |
AOS1 |
| Name |
Adams-Oliver syndrome, type 1 (AOS1) |
| OMIM ID |
100300 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
54 |
| Associated with 1 gene |
ARHGAP31 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-05-28 22:59:49 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|