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Biotin metabolic disease

MONDO:0020699

A deficiency in biotin through either inherited or acquired causes.

4 clinical trials for this condition and its sub-types, 0 tagged with Biotin metabolic disease itself.

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Where it sits in the disease tree

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Part of

↑ Disorder of organic acid metabolism (154) ↑ Sulfur metabolism disease (14)

Sub-types of Biotin metabolic disease

Inborn error of biotin metabolism 0 trials · 3 incl. sub-types
1 sub-type
- Multiple carboxylase deficiency 0 trials · 3 incl. sub-types Sub-types →
Nutritional biotin deficiency 0 trials

Most studied deeper sub-types

Biotinidase deficiency (3) Holocarboxylase synthetase deficiency (1)

Including sub-types (4) Tagged with Biotin metabolic disease (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.