OBO ID: DOID:0080481
Term Name: peroxisome biogenesis disorder 6A Search Ontology:
Synonyms:
  • peroxisome biogenesis disorder 6A (Zellweger)
Definition: A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX10 gene on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/17055079
References:
Ontology: Human Disease   ( DOID:0080481 )
Relationships
is a type of:
OTHER peroxisome biogenesis disorder 6A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PEX10 Peroxisome biogenesis disorder 6A (Zellweger) 614870
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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