| Metadata | |
|---|---|
| ID | DOID:0080486 |
| Name | peroxisome biogenesis disorder 12A |
| Definition | A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX19 gene on chromosome 1q23. https://www.ncbi.nlm.nih.gov/pubmed/17055079 |
| Xrefs | |
| Synonyms |
peroxisome biogenesis disorder 12A (Zellweger) [EXACT] |
| Parent Relationships |
is_a Zellweger syndrome |