| Term Name: | peroxisome biogenesis disorder 3B |
|---|---|
| Synonyms: | |
| Definition: | A peroxisome biogenesis disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PEX12 gene on chromosome 17. |
| Ontology: | Human Disease [DOID:0081241] ( DOID:0081241 ) |