Disease #03759 (PBD5A (peroxisome biogenesis disorder, type 5A (PBD-5A)), OMIM:614866)

Official abbreviation PBD5A
Name peroxisome biogenesis disorder, type 5A (PBD-5A)
OMIM ID 614866
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PEX2
Associated tissues -
Disease features -
Remarks -

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