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familial syringomyelia

Disease Summary
Associated Targets (0)

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Mondo Description An instance of syringomyelia that is caused by an inherited modification of the individual's genome.
Mondo Term and Equivalent IDs
MONDO:0018257:  familial syringomyelia
Orphanet:370034: 
UMLS:CN204832: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found