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MIM:614866 - PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER); PBD5A
Xenbase Genes: pex2
Human Disease Resource: MIM
MONDO:0013932 - peroxisome biogenesis disorder 5A (Zellweger) |
MONDO:0019609 - Zellweger spectrum disorders |
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MONDO:0013932 - peroxisome biogenesis disorder 5A (Zellweger) |
MONDO:0019609 - Zellweger spectrum disorders |