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Biotin metabolic disease

MONDO:0020699

A deficiency in biotin through either inherited or acquired causes.

13 clinical trials for this condition and its sub-types.

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Sub-types

Biotinidase deficiency (3) Holocarboxylase synthetase deficiency (1) Inborn error of biotin metabolism (0) Multiple carboxylase deficiency (0) Nutritional biotin deficiency (0)

Broader categories

Disease (618) Metabolic disease (215) Human disease (14) Mineral metabolism disease (1) Disease by developmental or physiological process (0) Disorder of organic acid metabolism (0) Sulfur metabolism disease (0)

Trials to join now! 10 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1

Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 03, 2026 00:00 UTC