OBO ID: DOID:2582
Term Name: acatalasia Search Ontology:
Synonyms:
  • acatalasemia
  • deficiency of catalase
Definition: A peroxisomal disease characterized by loss of catalase activity in erythrocytes that has_material_basis_in homozygous mutation in the CAT gene on chromosome 11p13. https://pubmed.ncbi.nlm.nih.gov/1999334/
References:
Ontology: Human Disease   ( DOID:2582 )
Relationships
is a type of:
OTHER acatalasia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CAT Acatalasemia 614097
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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