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ONTOLOGY REPORT - ANNOTATIONS


Term:Ogden syndrome
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Accession:DOID:0050781 term browser browse the term
Definition:An X-linked disease 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-TERMINAL ACETYLTRANSFERASE DEFICIENCY;   N-alpha-acetyltransferase;   NATD;   OGDNS;   X-linked Malformation and Infantile Lethality Syndrome
 primary_id: OMIM:300855
 alt_id: RDO:9000620
For additional species annotation, visit the Alliance of Genome Resources.


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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
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14924
    syndrome 4713
      Ogden syndrome 1
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      nervous system disease 9141
        central nervous system disease 6931
          brain disease 6435
            disease of mental health 4324
              Neurodevelopmental Disorders 2761
                Developmental Disabilities 346
                  Ogden syndrome 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.