LEOPARD Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_14291)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D044542
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Genes

4 genes/proteins associated with the disease LEOPARD Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PTPN11 protein tyrosine phosphatase, non-receptor type 11 2.88009
EPHA2 EPH receptor A2 2.88009
RAF1 Raf-1 proto-oncogene, serine/threonine kinase 2.88009
PTEN phosphatase and tensin homolog 2.88009