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Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2

MONDO:0980701

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

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Broader categories

Disease (717) Metabolic disease (241) Hereditary disease (188) Eye disorder (104) Inborn errors of metabolism (47) Human disease (15) Lens disorder (12) Developmental defect during embryogenesis (8) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2)

Trials to join now! 1 Completed 1

NIH launches major study to unlock secrets of rare bone diseases

Knowledge-focused Recruiting now

This study aims to collect information and bone samples from up to 1,000 people with bone or mineral disorders, such as tumor-induced osteomalacia or familial tumoral calcinosis. Participants receive standard medical evaluations and may provide bone tissue from surgery or a biops…

Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused

Last updated Sep 03, 2026 00:00 UTC