OBO ID: DOID:0111164
Term Name: molybdenum cofactor deficiency type A Search Ontology:
Synonyms:
  • combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type A
  • MOCOD type A
  • MOCODA
  • molybdenum cofactor deficiency complementation group A
Definition: A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS1 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/9731530
References:
Ontology: Human Disease   ( DOID:0111164 )
Relationships
is a type of:
OTHER molybdenum cofactor deficiency type A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MOCS1 Molybdenum cofactor deficiency A 252150
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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