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GTR Home > Conditions/Phenotypes > Multiple synostoses syndrome 3

Multiple synostoses syndrome 3

Summary

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

Available tests

8 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: FGF-9, GAF, HBFG-9, HBGF-9, SYNS3, FGF9
    Summary: fibroblast growth factor 9

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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