Disease #04016 (VRJS (Verheij syndrome (chromosome deletion syndrome 8q24.3)), OMIM:615583)
| Official abbreviation |
VRJS |
| Name |
Verheij syndrome (chromosome deletion syndrome 8q24.3) |
| OMIM ID |
615583 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
11 |
| Phenotype entries for this disease |
10 |
| Associated with 1 gene |
PUF60 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2024-02-23 15:08:27 +01:00 (CET) |
Individuals
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