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MIM:614872 - PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A
Xenbase Genes: pex26
Human Disease Resource: MIM
MONDO:0013938 - peroxisome biogenesis disorder 7A (Zellweger) |
MONDO:0019609 - Zellweger spectrum disorders |
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MONDO:0013938 - peroxisome biogenesis disorder 7A (Zellweger) |
MONDO:0019609 - Zellweger spectrum disorders |