Disease #01703 (PBD2A (peroxisome biogenesis disorder, type 2A (PBD2A)), OMIM:214110)

Official abbreviation PBD2A
Name peroxisome biogenesis disorder, type 2A (PBD2A)
OMIM ID 214110
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 PEX5
Associated tissues -
Disease features -
Remarks -

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