Disease #03755 (PBD3A (peroxisome biogenesis disorder, type 3A (PBD-3A)), OMIM:614859)

Official abbreviation PBD3A
Name peroxisome biogenesis disorder, type 3A (PBD-3A)
OMIM ID 614859
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 PEX12
Associated tissues -
Disease features -
Remarks -

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