mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615381
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Genes

1 genes associated with the mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
POLD1 polymerase (DNA directed), delta 1, catalytic subunit