| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A syndrome that is characterized by intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities and has_physical_basis_in heterozygous mutation in the CDKN1C gene. (Human Disease Ontology, DOID_0050885) |
| External Link | http://www.omim.org/entry/614732 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the image syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CDKN1C | cyclin-dependent kinase inhibitor 1C (p57, Kip2) |
