Search Ontology:
Human Disease

holocarboxylase synthetase deficiency

Term ID
DOID:859
Synonyms
  • Biotin-(propionyl-CoA-carboxylase) ligase deficiency
  • Multiple carboxylase deficiency - neonatal onset
Definition
A multiple carboxylase deficiency that involves a deficiency in holocarboxylase synthetase. http://en.wikipedia.org/wiki/Multiple_carboxylase_deficiency
References
Ontology
Human Disease   ( DOID:859 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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