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Desmosterolosis

MONDO:0011217

Desmosterolosis is a very rare sterol biosynthesis disorder characterized by multiple congenital anomalies, failure to thrive, and intellectual disability, with elevated levels of desmosterol.

Also known as: desmosterolosis

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

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Broader categories

Disease (680) Metabolic disease (233) Musculoskeletal system disorder (207) Inherited lipid metabolism disorder (189) Hereditary disease (176) Bone disorder (51) Inborn errors of metabolism (45) Human disease (14) Osteochondrodysplasia (12) Developmental defect during embryogenesis (8)
Trials to join now! 1 Terminated 1
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  • Scientists dive into rare cholesterol disorders to uncover clues

    Knowledge-focused Terminated

    This study looks at rare genetic disorders where the body can't make cholesterol properly, which can cause birth defects and learning problems. Researchers collect blood, urine, and tissue samples from affected people and their families to learn more about these conditions. The g…

    Sponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) • Aim: Knowledge-focused

    Last updated Aug 14, 2026 00:00 UTC

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