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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