biotinidase deficiency
Sign in to saveAlso known as BTD deficiency, deficiency of biotinidase (disorder), deficiency of biotinidase, juvenile-onset multiple carboxylase deficiency, late-onset multiple carboxylase deficiency, multiple carboxylase deficiency, juvenile-onset, multiple carboxylase deficiency, late-onset
multiple carboxylase deficiency that involves a deficiency in biotinidase
In the Vinony graph
Within Vinony's link graph, biotinidase deficiency is referenced by 53 other articles, and connects out to biotinidase, protein and carbohydrate.
It is catalogued under topics including Autosomal recessive disorders, Rare diseases and Vitamin, coenzyme, and cofactor metabolism disorders.
Its subject is documented across 9 Wikipedia language editions.
Research
751 papers- Biotinidase Deficiency.1993
- Biotinidase deficiency.Advances in pediatrics · 1991
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.Pediatric health, medicine and therapeutics · 2020
- Biotinidase Deficiency.2026
- A Rare Biotinidase Deficiency in the Pediatrics Population: Genotype-Phenotype Analysis.Journal of pediatric genetics · 2023
via PubMed
Wikidata facts
- Image
- Biotin structure.svg
Show 5 more facts
- NCI Thesaurus ID
- C84598
- health specialty
- endocrinology
- exact match
- www.orpha.net/ORDO/Orphanet_79241
- ICD-9-CM
- 277.6
- on focus list of Wikimedia project
- WikiProject Medicine
Sources (8)
via Wikidata · CC0