Disease #05766 (MVA3 (mosaic variegated aneuploidy syndrome, type 3 (MVA3)), OMIM:617598)
| Official abbreviation |
MVA3 |
| Name |
mosaic variegated aneuploidy syndrome, type 3 (MVA3) |
| OMIM ID |
617598 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TRIP13 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-06-09 08:59:04 +02:00 (CEST) |
| Date last edited |
N/A |
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