pseudoachondroplasia Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An osteochondrodysplasia that has_material_basis_in mutations in the COMP gene which results_in short limb dwarfism. (Human Disease Ontology, DOID_0080047)
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Genes

1 genes involed in the disease pseudoachondroplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
COMP cartilage oligomeric matrix protein