Human genes for Ogden syndrome
Ogden syndrome [DOID:0050781]
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.
Synonyms: Ogden syndrome, DOID:0050781, Ogden disease, Ogden disorder, Ogden syndromes ...