Disease #03774 (PBD10A (peroxisome biogenesis disorder, type 10A (PBD-10A)), OMIM:614882)

Official abbreviation PBD10A
Name peroxisome biogenesis disorder, type 10A (PBD-10A)
OMIM ID 614882
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 PEX3
Associated tissues -
Disease features -
Remarks -

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