Search Ontology:
Human Disease

peroxisome biogenesis disorder 2B

Term ID
DOID:0080622
Synonyms
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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