| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An osteochondrodysplasia that has_material_basis_in mutations in the COMP gene which results_in short limb dwarfism. (Human Disease Ontology, DOID_0080047) |
| External Link | http://www.omim.org/entry/177170 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the pseudoachondroplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| COMP | cartilage oligomeric matrix protein |
