Disease #04180 (AOS5 (Adams-Oliver syndrome, type 5 (AOS-5)), OMIM:616028)
Official abbreviation |
AOS5 |
Name |
Adams-Oliver syndrome, type 5 (AOS-5) |
OMIM ID |
616028 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
NOTCH1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-02-07 16:01:19 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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