Melorheostosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An osteosclerosis that has_material_basis_in a mutation of the LEMD3 gene which results_in a hyperdense bony cortex. (Human Disease Ontology, DOID_4253)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D008557
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Genes

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

Symbol Name Standardized Value
LEMD3 LEM domain containing 3 2.88009