| Dataset | CTD Gene-Disease Associations |
| 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) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C535819 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Pseudoachondroplasia from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| COMP | cartilage oligomeric matrix protein | 2.88009 |
