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Familial syringomyelia

MONDO:0018257

An instance of syringomyelia that is caused by an inherited modification of the individual's genome.

Also known as: hereditary syringomyelia

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

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Central nervous system disorder (97) Spinal cord disorder (38) Human disease (14) Hereditary neurological disease (5) Syringomyelia (5) Disease of genetic or genomic mechanism (2) Disease by body system or component (0)

Trials to join now! 1 Not yet finished but already full! 1

AI boosts brain scan accuracy in massive new trial

Diagnosis ENROLLING_BY_INVITATION

This study tests whether an AI tool can help radiologists read brain CT and MRI scans more accurately and quickly. Researchers will compare how well doctors, AI alone, and doctors using AI together can spot abnormalities, urgent findings, and classify diseases. The goal is to red…

Sponsor: Yaou Liu • Aim: Diagnosis

Last updated Jun 27, 2026 11:00 UTC