Osteochondroma Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description greater than the expected number of a benign cartilagenous neoplasm that consists of a pedicle of normal bone capped by a region of proliferating cartilage cells, occurring in a specific population in a given time period; osteochondroma is most often associated with one or more of the long bones (Mammalian Phenotype Ontology, MP_0010079)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D015831
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Genes

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

Symbol Name Standardized Value
PTPN11 protein tyrosine phosphatase, non-receptor type 11 2.88009