Osteopetrosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An osteosclerosis that has_material_basis_in lack of bone resorption which results_in abnormally hard and brittle bones. (Human Disease Ontology, DOID_13533)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D010022
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Genes

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

Symbol Name Standardized Value
FERMT3 fermitin family member 3 2.88009
CLCN7 chloride channel, voltage-sensitive 7 2.88009
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11 2.88009