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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

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

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Central nervous system disorder (107) Spinal cord disorder (43) Human disease (14) Hereditary neurological disease (6) Syringomyelia (6) Disease of genetic or genomic mechanism (2) Disease by body system or component (0)

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