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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