|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Acromicric dysplasia is a rare bone dysplasia characterized by short stature, short hands and feet, mild facial dysmorphism, and characteristic X-ray abnormalities of the hands. (Orphanet Rare Disease Ontology, Orphanet_969)|
|Downloads & Tools|
3 genes/proteins associated with the disease Acromicric dysplasia from the curated CTD Gene-Disease Associations dataset.