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CYP7B1-related disorder of oxysterol accumulation

MONDO:1060107

Any disorder of oxysterol accumulation caused by biallelic loss of function variants in the CYP7B1 gene. A disorder of oxysterol accumulation is a condition where there is an abnormal buildup of oxysterols, which are oxidized cholesterol derivatives, in the body.

Also known as: CYP7B1-related disorder of oxysterol accumulation

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

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Sub-types

Hereditary spastic paraplegia 5A (2) Congenital bile acid synthesis defect 3 (0)

Broader categories

Disease (680) Metabolic disease (233) Inherited lipid metabolism disorder (189) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0)
Trials to join now! 1 Completed 1
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  • Researchers launch study to understand rare paralysis conditions

    Knowledge-focused Recruiting now

    This study is collecting health data and blood samples from 100 people with specific types of hereditary spastic paraplegia (SPG4 and SPG5A). The goal is to create a shared database and biobank to better understand how the disease progresses. This information will help prepare fo…

    Sponsor: Boston Children's Hospital • Aim: Knowledge-focused

    Last updated Jun 27, 2026 11:03 UTC

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