Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

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.

Follow this condition — get notified about new trials

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
Sort by
  • New study aims to unlock secrets of rare cholesterol diseases

    Knowledge-focused Recruiting now

    This natural history study is observing up to 250 people with Smith-Lemli-Opitz syndrome and related cholesterol disorders, as well as their relatives. Researchers will track symptoms, development, and lab results over several years to find better ways to measure disease progress…

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

    Last updated Aug 18, 2026 04:00 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space