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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

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
 xref: NCI:C188215
For additional species annotation, visit the Alliance of Genome Resources.

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Ogden syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit ISO ClinVar Annotator: match by term: Ogden syndrome OMIM
PMID:18414213 PMID:21700266 PMID:23020937 PMID:25099252 PMID:25326635 More... NCBI chr  X:151,656,056...151,661,304
Ensembl chr  X:151,656,056...151,661,252
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18246
    syndrome 9798
      Ogden syndrome 1
Path 2
Term Annotations click to browse term
  disease 18246
    disease of anatomical entity 17610
      nervous system disease 13264
        central nervous system disease 11415
          brain disease 10712
            disease of mental health 7590
              Neurodevelopmental Disorders 6220
                Developmental Disabilities 691
                  Ogden syndrome 1
paths to the root