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Term:Ogden syndrome
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Accession:DOID:0050781 term browser browse the term
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. (DO)
Synonyms:exact_synonym: N-alpha-acetyltransferase;   N-terminal acetyltransferase deficiency;   NATD;   OGDNS;   X-linked malformation and infantile lethality syndrome
 primary_id: OMIM:300855
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Ogden syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit JBrowse link X 156,863,655 156,868,950 RGD:7240710

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Path 1
Term Annotations click to browse term
  disease 15503
    syndrome 5771
      Ogden syndrome 1
Path 2
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  disease 15503
    disease of anatomical entity 14857
      nervous system disease 10273
        central nervous system disease 8410
          brain disease 7763
            disease of mental health 5617
              Neurodevelopmental Disorders 4162
                Developmental Disabilities 379
                  Ogden syndrome 1
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