OBO ID: DOID:0080483
Term Name: peroxisome biogenesis disorder 8A Search Ontology:
Synonyms:
  • peroxisome biogenesis disorder 8A (Zellweger)
Definition: A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX16 gene on chromosome 11p11. https://www.ncbi.nlm.nih.gov/pubmed/17055079
References:
Ontology: Human Disease   ( DOID:0080483 )
Relationships
is a type of:
OTHER peroxisome biogenesis disorder 8A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PEX16 Peroxisome biogenesis disorder 8A (Zellweger) 614876
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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