| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/102370 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the acromicric dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| FBN1 | fibrillin 1 |
