OBO ID: DOID:0080622
Term Name: peroxisome biogenesis disorder 2B Search Ontology:
Synonyms:
Definition: A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13.3. https://www.ncbi.nlm.nih.gov/pubmed/22871920
References:
Ontology: Human Disease   ( DOID:0080622 )
Relationships
is a type of:
OTHER peroxisome biogenesis disorder 2B PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PEX5 Peroxisome biogenesis disorder 2B 202370
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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