3.6.4.6	medicine	diagnosis, HsPex6p mutations are one of the causes of Zellweger syndrome	210580	
3.6.4.6	medicine	dysfunction of p97 has serious pathological consequences and has been implicated in a variety of cancers and neurodegenerative deseases	688690	
3.6.4.6	medicine	HsPEX1 is the causative gene for peroxisome-deficiency autosomal recessive disorders like cerebro-hepato-renal Zellweger syndrome, neonatal adrenoleukodystrophy and infantile refsum disease	210581, 210583