Term Name: peroxisome biogenesis disorder 2B
Synonyms:
Definition: A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13.3.
Ontology: Human Disease [DOID:0080622]   ( DOID:0080622 )

Relationships
is a type of: autosomal recessive disease peroxisomal biogenesis disorder