Disease #00989 (BOS3 (branchiootic syndrome, type 3), OMIM:608389)
Official abbreviation |
BOS3 |
Name |
branchiootic syndrome, type 3 |
OMIM ID |
608389 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SIX1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2022-01-23 14:00:37 +01:00 (CET) |
|
|