Search Ontology:
Human Disease

peroxisome biogenesis disorder 3A

Term ID
DOID:0080478
Synonyms
  • peroxisome biogenesis disorder 3A (Zellweger)
Definition
A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX12 gene on chromosome 17. https://www.ncbi.nlm.nih.gov/pubmed/17055079
References
Ontology
Human Disease   ( DOID:0080478 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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