Campomelic Dysplasia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An osteochondrodysplasia that has_material_basis_in a mutation in chromosome 17 which results_in bowing in the located_in tibia or located_in femur. (Human Disease Ontology, DOID_0050463)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D055036
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Genes

1 genes/proteins associated with the disease Campomelic Dysplasia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SOX9 SRY (sex determining region Y)-box 9 2.88009