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- Q776026 subject Q15127406.
- Q776026 subject Q6902466.
- Q776026 abstract "Biotinidase deficiency is an autosomal recessive metabolic disorder in which biotin is not released from proteins in the diet during digestion or from normal protein turnover in the cell. This situation results in biotin deficiency.Biotin, also called vitamin B7, is an important water-soluble nutrient that aids in the metabolism of fats, carbohydrates, and proteins. Biotin deficiency can result in behavioral disorders, lack of coordination, learning disabilities and seizures. Biotin supplementation can alleviate and sometimes totally arrest such symptoms.".
- Q776026 icd10 "E53.8".
- Q776026 icd9 "277.6".
- Q776026 meshId "D028921".
- Q776026 omim "253260".
- Q776026 thumbnail Biotin_structure.svg?width=300.
- Q776026 wikiPageExternalLink BTD_welcome.php.
- Q776026 wikiPageExternalLink 253260,253260,609019,253260,609019.
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- Q776026 wikiPageWikiLink Q15127406.
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- Q776026 wikiPageWikiLink Q6902466.
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- Q776026 icd "277.6".
- Q776026 icd "E53.8".
- Q776026 meshid "D028921".
- Q776026 name "Biotinidase deficiency".
- Q776026 omim "253260".
- Q776026 type Disease.
- Q776026 type Thing.
- Q776026 type Q12136.
- Q776026 comment "Biotinidase deficiency is an autosomal recessive metabolic disorder in which biotin is not released from proteins in the diet during digestion or from normal protein turnover in the cell. This situation results in biotin deficiency.Biotin, also called vitamin B7, is an important water-soluble nutrient that aids in the metabolism of fats, carbohydrates, and proteins. Biotin deficiency can result in behavioral disorders, lack of coordination, learning disabilities and seizures.".
- Q776026 label "Biotinidase deficiency".
- Q776026 depiction Biotin_structure.svg.
- Q776026 name "Biotinidase deficiency".