| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An abnormality of the process of endochondral ossification, which is a type of replacement ossification in which bone tissue replaces cartilage. (Human Phenotype Ontology, HP_0003336) |
| External Link | https://www.disgenet.org/browser/0/1/0/C4025628 |
| Similar Terms | |
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4 genes associated with the disease Abnormal Enchondral Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
