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Biotin deficiency MeSH Supplementary Concept Data 2024


MeSH Supplementary
Biotin deficiency
Unique ID
C531633
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C531633
Registry Number
0
Heading Mapped to
*Biotinidase Deficiency
Frequency
106
Note
Rare definiciency in BIOTIN caused by mutations in the biotinidase (BTD) gene or genes for other enzymes involved in biotin metabolism. OMIM: 253260
Date of Entry
2010/08/25
Revision Date
2019/06/20
Biotin deficiency Preferred
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