OBO ID: DOID:0050781
Term Name: Ogden syndrome Search Ontology:
Synonyms:
  • N-alpha-acetyltransferase
  • N-terminal acetyltransferase deficiency
  • OGDNS
  • X-linked Malformation and Infantile Lethality Syndrome
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)
References:
Ontology: Human Disease   (DOID:0050781)
OTHER Ogden syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NAA10 Ogden syndrome 300855
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None