Disease #06723 (POBINDS (Poirier-Bienvenu neurodevelopmental syndrome), OMIM:618732)
| Official abbreviation |
POBINDS |
| Name |
Poirier-Bienvenu neurodevelopmental syndrome |
| OMIM ID |
618732 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
CSNK2B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|