Disease #05465 (del 22q11.2 (chromosome deletion syndrome 22q11.2, distal), OMIM:611867)
| Official abbreviation |
del 22q11.2 |
| Name |
chromosome deletion syndrome 22q11.2, distal |
| OMIM ID |
611867 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2018-08-04 00:00:12 +02:00 (CEST) |
| Date last edited |
2022-09-08 15:28:52 +02:00 (CEST) |
Individuals
|