weill-marchesani syndrome 2, dominant Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/608328
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Genes

1 genes associated with the weill-marchesani syndrome 2, dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
FBN1 fibrillin 1