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MIM:614883 - PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER); PBD11A
Xenbase Genes: pex13
Human Disease Resource: MIM
MONDO:0013949 - peroxisome biogenesis disorder 11A (Zellweger) |
MONDO:0019609 - Zellweger spectrum disorders |
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MONDO:0013949 - peroxisome biogenesis disorder 11A (Zellweger) |
MONDO:0019609 - Zellweger spectrum disorders |