|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An osteochondrodysplasia that has_material_basis_in abnormal cartilage development due to mutations in the SLC26A2 gene which results_in short limb dwarfism. (Human Disease Ontology, DOID_14687)|
|Downloads & Tools|
1 genes associated with the diastrophic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
|SLC26A2||solute carrier family 26 (anion exchanger), member 2|