OBO ID: DOID:0080484
Term Name: peroxisome biogenesis disorder 10A Search Ontology:
Synonyms:
  • peroxisome biogenesis disorder 10A (Zellweger)
Definition: A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX3 gene on chromosome 6q24. https://www.ncbi.nlm.nih.gov/pubmed/17055079
References:
Ontology: Human Disease   ( DOID:0080484 )
Relationships
is a type of:
OTHER peroxisome biogenesis disorder 10A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PEX3 Peroxisome biogenesis disorder 10A (Zellweger) 614882
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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