OBO ID: DOID:0080487
Term Name: peroxisome biogenesis disorder 13A Search Ontology:
Synonyms:
  • peroxisome biogenesis disorder 13A (Zellweger)
Definition: A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX14 gene on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/17055079
References:
Ontology: Human Disease   ( DOID:0080487 )
Relationships
is a type of:
OTHER peroxisome biogenesis disorder 13A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PEX14 Peroxisome biogenesis disorder 13A (Zellweger) 614887
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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