| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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 | http://www.omim.org/entry/300855 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the n-terminal acetyltransferase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| NAA10 | N(alpha)-acetyltransferase 10, NatA catalytic subunit |
