| Term Name: | Ogden syndrome |
|---|---|
| Synonyms: | N-alpha-acetyltransferase, N-terminal acetyltransferase deficiency, OGDNS, X-linked Malformation and Infantile Lethality Syndrome |
| Definition: | A syndrome characterized by postnatal growth failure, severely delayed psychomotor development, variable dysmorphic features, and hypotonia and has_material_basis_in X-linked recessive or X-linked dominant mutation in the NAA10 gene on chromosome Xq28. |
| Ontology: | Human Disease [DOID:0050781] ( DOID:0050781 ) |