Structured Summary
Abstract
The late onset form of MULTIPLE CARBOXYLASE DEFICIENCY (deficiency of the activities of biotin-dependent enzymes propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, and PYRUVATE CARBOXYLASE) due to a defect or deficiency in biotinidase which is essential for recycling BIOTIN.
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Broader headings
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Synonyms
15 entry terms
- BTD Deficiency
- Carboxylase Deficiency, Multiple, Late-Onset
- Deficiency, Biotinidase
- Deficiency, Multiple Carboxylase, Late-Onset
- Late-Onset Biotin-Responsive Multiple Carboxylase Deficiency
- Late-Onset Multiple Carboxylase Deficiency
- Multiple Carboxylase Deficiency, Late-Onset
- BTD Deficiencies
- Biotinidase Deficiencies
- Deficiencies, BTD
- Deficiencies, Biotinidase
- Deficiency, BTD
- Late Onset Biotin Responsive Multiple Carboxylase Deficiency
- Late Onset Multiple Carboxylase Deficiency
- Multiple Carboxylase Deficiency, Late Onset
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2002
MeSH Record
Previous Indexing
- Amidohydrolases/deficiency (1983-2001)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Biotinidase Deficiency. Medical Subject Headings (MeSH). 2026. Unique ID D028921. http://id.nlm.nih.gov/mesh/2026/D028921
- Biotinidase Deficiency. In: Wikipedia. https://en.wikipedia.org/wiki/Biotinidase_deficiency
- Biotinidase Deficiency. In: Wikidata. https://www.wikidata.org/wiki/Q776026