| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An X-linked disease resulting from a deficiency in N-terminal acetyltransferase, characterized by postnatal growth failure with severe delays and dysmorphic features in boys. (Human Disease Ontology, DOID_0050781) |
| External Link | https://www.disgenet.org/browser/0/1/0/C3275447 |
| Similar Terms | |
| Downloads & Tools |
6 genes associated with the disease Ogden Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ARHGAP4 | Rho GTPase activating protein 4 |
| BRD2 | bromodomain containing 2 |
| DNMT1 | DNA (cytosine-5-)-methyltransferase 1 |
| NAA10 | N(alpha)-acetyltransferase 10, NatA catalytic subunit |
| NAA15 | N(alpha)-acetyltransferase 15, NatA auxiliary subunit |
| NAA50 | N(alpha)-acetyltransferase 50, NatE catalytic subunit |
