Ogden syndrome (DOID:0050781)
Alliance: disease page
Synonyms: N-alpha-acetyltransferase; N-terminal acetyltransferase deficiency; OGDNS; X-linked Malformation and Infantile Lethality Syndrome
Alt IDs: OMIM:300855, ORDO:276432
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.