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Disease Ontology Browser
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory