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Human Disease

Ogden syndrome

Term ID
DOID:0050781
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. (2)
References
Ontology
Human Disease   ( DOID:0050781 )
Relationships
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Genes Involved
Zebrafish Models