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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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

Below are MeSH descriptors whose meaning is more general than "Multiple Carboxylase Deficiency".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
Multiple Carboxylase Deficiency [C16.320.565.100.620]
Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
Multiple Carboxylase Deficiency [C16.320.565.202.720]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
Multiple Carboxylase Deficiency [C18.452.648.100.620]
Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
Multiple Carboxylase Deficiency [C18.452.648.202.720]

Below are MeSH descriptors whose meaning is related to "Multiple Carboxylase Deficiency".

Below are MeSH descriptors whose meaning is more specific than "Multiple Carboxylase Deficiency".

publications

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This graph shows the total number of publications written about "Multiple Carboxylase Deficiency" by people in Harvard Catalyst Profiles by year, and whether "Multiple Carboxylase Deficiency" was a major or minor topic of these publication.

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