Disease #03769 (PBD8B (peroxisome biogenesis disorder, type 8B (PBD-8B)), OMIM:614877)

Official abbreviation PBD8B
Name peroxisome biogenesis disorder, type 8B (PBD-8B)
OMIM ID 614877
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 PEX16
Associated tissues -
Disease features -
Remarks -

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