Multiple Carboxylase Deficiency
"Multiple Carboxylase Deficiency" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A deficiency in the activities of biotin-dependent enzymes (propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, and PYRUVATE CARBOXYLASE) due to one of two defects in BIOTIN metabolism. The neonatal form is due to HOLOCARBOXYLASE SYNTHETASE DEFICIENCY. The late-onset form is due to BIOTINIDASE DEFICIENCY.
| Descriptor ID |
D009100
|
| MeSH Number(s) |
C16.320.565.100.620 C16.320.565.202.720 C18.452.648.100.620 C18.452.648.202.720
|
| Concept/Terms |
Multiple Carboxylase Deficiency- Multiple Carboxylase Deficiency
- Carboxylase Deficiencies, Multiple
- Deficiencies, Multiple Carboxylase
- Multiple Carboxylase Deficiencies
- Deficiency, Combined Carboxylase
- Deficiency, Multiple Carboxylase
- Carboxylase Deficiency, Multiple
- Carboxylase Deficiency, Combined
- Carboxylase Deficiencies, Combined
- Combined Carboxylase Deficiencies
- Deficiencies, Combined Carboxylase
- Combined Carboxylase Deficiency
|
Below are MeSH descriptors whose meaning is more general than "Multiple Carboxylase Deficiency".
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