Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B1

MONDO:0009644

Also known as: MOCOD type B, MOCODB, combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B, molybdenum cofactor deficiency B, molybdenum cofactor deficiency, complementation group type B, sulfite oxidase deficiency due to molybdenum cofactor deficiency type B, molybdenum cofactor deficiency type B, molybdenum cofactor deficiency, complementation group B

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

AI eye chatbot matches doctors in taking patient history

Knowledge-focused Completed

This study tested whether a large language model (like ChatGPT) could collect medical history and suggest eye tests as well as doctors do. 172 patients with non-emergency eye problems took part. The AI's performance was compared to standard care, with senior specialists checking …

Sponsor: Zhongshan Ophthalmic Center, Sun Yat-sen University • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:10 UTC

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B1

Broader categories

AI eye chatbot matches doctors in taking patient history