OBO ID: DOID:0080478
Term Name: peroxisome biogenesis disorder 3A Search Ontology:
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 peroxisome biogenesis disorder 3A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PEX12 Peroxisome biogenesis disorder 3A (Zellweger) 614859
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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