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holocarboxylase synthetase deficiency (DOID:859)
Alliance: disease page
Synonyms: Biotin-(propionyl-CoA-carboxylase) ligase deficiency; Multiple carboxylase deficiency - neonatal onset
Alt IDs: OMIM:253270, ICD10CM:D81.818, MESH:D028922, NCI:C98842, NCI:C99247, UMLS_CUI:C0268581
Definition: A multiple carboxylase deficiency that involves a deficiency in holocarboxylase synthetase.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory