OBO ID: DOID:0050781 |
Term Name: | Ogden syndrome | Search Ontology: | |
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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. (2) | ||
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Ontology: | Human Disease ( DOID:0050781 ) |
OTHER Ogden syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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