Disease #01634 (PBD2B (peroxisome biogenesis disorder, type 2B (PBD2B)), OMIM:202370)

Official abbreviation PBD2B
Name peroxisome biogenesis disorder, type 2B (PBD2B)
OMIM ID 202370
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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