Disease #03776 (PBD11B (peroxisome biogenesis disorder, type 11B (PBD-11B)), OMIM:614885)

Official abbreviation PBD11B
Name peroxisome biogenesis disorder, type 11B (PBD-11B)
OMIM ID 614885
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 PEX13
Associated tissues -
Disease features -
Remarks -

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