|OBO ID: DOID:0050781|
|Term Name:||Ogden syndrome||Search Ontology:|
|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. (3)|
|Ontology:||Human Disease (DOID:0050781)|
|is a type of:||
OTHER Ogden syndrome PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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