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MIM:614882 - PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A
Xenbase Genes: pex3
Human Disease Resource: MIM
MONDO:0013948 - peroxisome biogenesis disorder 10A (Zellweger) |
MONDO:0019609 - Zellweger spectrum disorders |
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MONDO:0013948 - peroxisome biogenesis disorder 10A (Zellweger) |
MONDO:0019609 - Zellweger spectrum disorders |