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MIM:614887 - PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER); PBD13A
Xenbase Genes: pex14
Human Disease Resource: MIM
MONDO:0013952 - peroxisome biogenesis disorder 13A (Zellweger) |
MONDO:0019609 - Zellweger spectrum disorders |
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MONDO:0013952 - peroxisome biogenesis disorder 13A (Zellweger) |
MONDO:0019609 - Zellweger spectrum disorders |