OBO ID: DOID:0080485
Term Name: peroxisome biogenesis disorder 11A Search Ontology:
Synonyms:
  • peroxisome biogenesis disorder 11A (Zellweger)
Definition: A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX13 gene on chromosome 2p15. https://www.ncbi.nlm.nih.gov/pubmed/17055079
References:
Ontology: Human Disease   ( DOID:0080485 )
Relationships
is a type of:
OTHER peroxisome biogenesis disorder 11A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PEX13 Peroxisome biogenesis disorder 11A (Zellweger) 614883
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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