Disease table of PREMATURE AGING SYNDROME, PENTTINEN TYPE OMIM ID: 601812

Gene-disease associations table

GeneAssociated with PREMATURE AGING SYNDROME, PENTTINEN TYPE inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
PDGFRBOMIMHGNC link5q325PS228550, 601812, PS213600, 616592, 131440

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