Search Ontology:
Human Disease
peroxisome biogenesis disorder 2B
- Term ID
- DOID:0080622
- Synonyms
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- Definition
- A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13.3. https://www.ncbi.nlm.nih.gov/pubmed/22871920
- References
- Ontology
- Human Disease ( DOID:0080622 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models