Disease #05208 (JBS;11q (Jacobsen syndrome (JBS; deletion syndrome, chromosome 11q)), OMIM:147791)
| Official abbreviation |
JBS;11q |
| Name |
Jacobsen syndrome (JBS; deletion syndrome, chromosome 11q) |
| OMIM ID |
147791 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2016-12-06 21:38:27 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|