Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX19 gene.
Comprehensive, easy-to-understand information about this condition
Checking for content...
No external resources available.
peroxisome biogenesis disorder 9B
MONDO:0013945
peroxisome biogenesis disorder 12A (Zellweger)
MONDO:0013951
peroxisome biogenesis disorder due to PEX1 defect
MONDO:0100259
peroxisome biogenesis disorder due to PEX2 defect
MONDO:0100260
peroxisome biogenesis disorder due to PEX3 defect
MONDO:0100261
peroxisome biogenesis disorder due to PEX5 defect
MONDO:0100262