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