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.

Synonyms

N-alpha-acetyltransferase
N-terminal acetyltransferase deficiency

Cross References

Parent Terms

Child Terms

None

Sources of Associations

Associated Genes

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Associated Alleles

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Associated Models

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Ogden syndrome

Ogden syndrome

Associated Genes

Associated Alleles

Associated Models