hypochondroplasia 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 mutation in the FGFR3 gene which affects ossification of cartilage and results_in short limb dwarfism. (Human Disease Ontology, DOID_0080041)
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Genes

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

Symbol Name
FGFR3 fibroblast growth factor receptor 3