| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C535662 |
| Similar Terms | |
| Downloads & Tools |
3 genes/proteins associated with the disease Acromicric dysplasia from the curated CTD Gene-Disease Associations dataset.
