Disease #03763 (PBD6A (peroxisome biogenesis disorder, type 6A (PBD-6A)), OMIM:614870)

Official abbreviation PBD6A
Name peroxisome biogenesis disorder, type 6A (PBD-6A)
OMIM ID 614870
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 -