Disease #03771 (PBD9B (peroxisome biogenesis disorder, type 9B (PBD9B)), OMIM:614879)

Official abbreviation PBD9B
Name peroxisome biogenesis disorder, type 9B (PBD9B)
OMIM ID 614879
Human Phenotype Ontology Project (HPO) HPO
Inheritance AR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PEX7
Associated tissues -
Disease features -
Remarks -