OBO ID: DOID:0080477
Term Name: peroxisome biogenesis disorder 2A Search Ontology:
Synonyms:
  • peroxisome biogenesis disorder 2A (Zellweger)
Definition: A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13. https://www.ncbi.nlm.nih.gov/pubmed/17055079
References:
Ontology: Human Disease   ( DOID:0080477 )
Relationships
is a type of:
OTHER peroxisome biogenesis disorder 2A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PEX5 Peroxisome biogenesis disorder 2A (Zellweger) 214110
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.