Disease #03768 (PBD8A (peroxisome biogenesis disorder, type 8A (PBD-8A)), OMIM:614876)

Official abbreviation PBD8A
Name peroxisome biogenesis disorder, type 8A (PBD-8A)
OMIM ID 614876
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PEX16
Associated tissues -
Disease features -
Remarks -

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