/multiple synostoses syndrome 3

multiple synostoses syndrome 3

Rare Disease

MONDO:0013064

Also Known As

FGF9 multiple synostoses syndromemultiple synostoses syndrome 3multiple synostoses syndrome caused by mutation in FGF9multiple synostoses syndrome type 3SYNS3

Definition

Any multiple synostoses syndrome in which the cause of the disease is a mutation in the FGF9 gene.

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Comprehensive, easy-to-understand information about this condition

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Associated Genes

FGF9 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:612961 ↗

GARD

GARD:15597 ↗

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