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DOID:859 - holocarboxylase synthetase deficiency
Disease Ontology Definition:A multiple carboxylase deficiency that involves a deficiency in holocarboxylase synthetase.
Synonyms: Biotin-(propionyl-CoA-carboxylase) ligase deficiency (disorder), Multiple carboxylase deficiency - neonatal onset (disorder), Biotin-(propionyl-CoA-carboxylase) ligase deficiency, Multiple carboxylase deficiency - neonatal onset
Echinobase Genes
:
hlcs
| MIM:253270 - holocarboxylase synthetase deficiency |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
multiple carboxylase deficiency (is_a)