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
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