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Sulfite oxidase deficiency due to molybdenum cofactor deficiency

MONDO:0020480

Also known as: MOCOD, combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase, combined deficiency of sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase, molybdenum cofactor deficiency

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

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Sub-types

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (1) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B1 (0) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2 (0) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C (0)

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 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