Disease #03764 (PBD6B (peroxisome biogenesis disorder, type 6B (PBD-6B)), OMIM:614871)

Official abbreviation PBD6B
Name peroxisome biogenesis disorder, type 6B (PBD-6B)
OMIM ID 614871
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 PEX10
Associated tissues -
Disease features -
Remarks -

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