OBO ID: DOID:0080480
Term Name: peroxisome biogenesis disorder 5A Search Ontology:
Synonyms:
  • peroxisome biogenesis disorder 5A (Zellweger)
Definition: A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX2 gene on chromosome 8q21. https://www.ncbi.nlm.nih.gov/pubmed/17055079
References:
Ontology: Human Disease   ( DOID:0080480 )
Relationships
is a type of:
OTHER peroxisome biogenesis disorder 5A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PEX2 Peroxisome biogenesis disorder 5A (Zellweger) 614866
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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