Sterol biosynthesis disorder
MONDO:0019240An inherited metabolic disease that is has its basis in the disruption of sterol biosynthetic process.
Also known as: inborn error of sterol biosynthetic process, inborn sterol biosynthetic process disorder, rare inborn error of sterol biosynthetic process
45 clinical trials for this condition and its sub-types, 0 tagged with Sterol biosynthesis disorder itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Sterol biosynthesis disorder
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CHILD syndrome 37 trials
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Cholesterol biosynthetic process disease 2 trials · 6 incl. sub-types
3 sub-types
- Smith-Lemli-Opitz syndrome 6 trials
- Lathosterolosis 3 trials
- Desmosterolosis 2 trials
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Mevalonate kinase deficiency 3 trials · 4 incl. sub-types
2 sub-types
- Hyperimmunoglobulinemia D with periodic fever 2 trials
- Mevalonic aciduria 0 trials
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Greenberg dysplasia 2 trials
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2 sub-types
- X-linked chondrodysplasia punctata 2 1 trial
- X-linked chondrodysplasia punctata 1 0 trials
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MEND syndrome 0 trials
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Scientists dive into rare cholesterol disorders to uncover clues
Knowledge-focused Stopped earlyThis 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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Superhero training for food allergy safety falls short
Knowledge-focused Stopped earlyThis study aimed to help children aged 6-8 from low-income families learn how to avoid foods they are allergic to. The program used fun, hands-on activities to teach safety skills. The study was stopped early, so we don't have clear results on whether it worked.
Sponsor: Kent State University • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:23 UTC