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

Gene-disease associations table

Gene	Associated with PREMATURE AGING SYNDROME, PENTTINEN TYPE in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
PDGFRB	OMIM	HGNC link	5q32	5	PS228550, 601812, PS213600, 616592, 131440